All Activity

This stream auto-updates   

  1. Today
  2. What are the glyconegineering and glycosylation? Glycoengineering, as well as protein engineering and gene engineering, belongs to the category of biotechnology, and its basic research is also called glycobiology. The research of glycoengineering is still in the stage of basic and applied basic research. glycoengineering, which was born in 1990s, is a discipline to study the structure, function, metabolic regulation and application of glycoconjugates.With the research and elucidation of the biological functions of sugar chains, a variety of glycan antibodies are being developed, some of which have gone into clinical practice. Among many post-translational modifications of proteins, glycosylation modification is one of the most important and complex modifications, and also one of the key quality attributes for evaluating antibodies. The function of monoclonal antibodies is closely related to glycosylation modification. Glycosylation modification can affect the properties of proteins, such as conformation, stability, solubility, pharmacokinetics, activity and immunogenicity. Figure1.Types of glycosylation Different glycosylation modifications have different effects on the stability, half-life, safety and biological activity of the antagonists, which are described below. Stability and half-life The most obvious effect of glycosylation modification is that it can increase the stability and solubility of protein. Studies have shown that glycosylation protects proteins by hiding binding sites between proteins and proteases. Rudd et al found that the steric protection of N-glycosylation on adjacent polypeptides was due to the formation of hydrogen bonds between glycosylation and hydrophilic amino acids. Glycosylation modification can also hinder the binding of protease and antibody, thereby increasing the stability of antibody. Sialic acid glycosylation can prolong the existence time of glycoprotein in serum. When the glycoprotein chains are terminated by galactose modification or desalicitated, they can be recognized by the sialic glycoprotein receptor (ASGPR), resulting in a significant reduction in half-life. The ASGPR located on the surface of hepatocytes can not recognize the glycoprotein of total sialic acid, but it will be desalibrated by the non-specific sialidase in the blood as the blood circulates. The galactose glycosyl group of bare can be recognized by ASGPR, and the glycoprotein is degraded. Other studies suggest that high levels of mannose reduce the half-life of antibodies in serum. In general, the more stable the drug is in the body and the longer its half-life, the more effective it will be. As for antineoplastic drugs, if the stability of drugs is high and the half-life is long, the dosage can be reduced appropriately and the interval between doses can be designed longer, and the effect is the same. However, with the increase of drug stability and half-life in human body, drug safety will become one of the factors to be considered because of potential miss-target. Safety The key quality attributes of antibodies (CQAs) are the criteria to judge whether they are qualified or not. CQAs must be within an appropriate range to ensure the effectiveness of drugs and, more importantly, the safety of drugs. By influencing the effect function of Fc terminal, glycosylation modification of Fc terminal can affect the safety of antibodies in the form of immunogenicity, PK/PD. The development of antibodies has experienced the development of murine primordial antibody, chimeric antibody, humanized antibody, and finally the whole human antibody. The immunogenicity of antibodies has been continuously decreasing.Antibodies have developed into human antibodies, and the immunogenicity caused by different glycosylation modifications should not be considered. However, in order to increase the efficacy of antibodies or prolong their half-life, some amino acid mutations and glycosylation modifications are often introduced artificially, and their potential immunogenicity should be considered when making such modifications. Moreover, immunogenicity is not only caused by internal factors, but also by external factors such as materials, formation of polymers and introduction of surfactants. The main consideration of PK/PD is the minimum dose and time of drug action in vivo. It is particularly important to minimize the immunogenicity of antibodies that can not completely eliminate the immunogenicity. Glycosylation affects PK mainly by affecting the stability and half-life of antibodies. The effect of glycosylation on the activity of antibodies acts on PD, which will be discussed in the following sections. The clearance of antibodies that bind strongly to Fc receptor is low, and glycosylation can affect the binding strength of antibodies to Fc receptor or C1q complement. If the clearance rate of antibody is low, antibodies bound to Fc receptor or C1q complement may cause the immune system to attack normal cells, resulting in serious miss-target effect. Biological activity Antibody-dependent cell-mediated cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC) are two important pathways for the efficacy of antibodies in cancer therapy. The glycosylation modification sites of Fc end of antibody are usually the binding sites of Fc receptor (ADCC mechanism) and C1q (CDC mechanism). By adjusting glycosylation, the binding of Fc receptor and C1q with antibody can be increased, thus the activity of antibody ADCC and CDC can be increased.It has been reported in many studies that glycosylation of sialic acid can affect the binding of antibody to FcγRIIa, thus reducing the activity of ADCC. Figure2.Mechanisms of action of ADCC and CDC Conformation determines performance. The effects of glycosylation modification on the stability, half-life, safety and biological activity of antibiotics are cross-cutting. It is the best choice to control the glycosylation modification of antibodies within an appropriate range so as to balance the three. Expectation Drug glycosylation is a unique post-translational modification. Their synthesis is not a mode-driven process, so it is a difficult task to obtain a consistent glycosylation. Sugar forms are known to regulate a range of complex functions, and it is pertinent to invent strategies that are easy to monitor sugars in real time. In addition to significant progress in process analysis, glycosylation level control remains an unrealized goal. Biopharmaceutical industry and academic researchers have made great efforts to bridge this gap, and have made great progress in understanding the complexity of post-translational modification. They have also understood the effects of process variables on sugar types and the effects of polysaccharide types on the efficacy of biopharmaceuticals. This also clearly implies that in the development of bio-analogue drugs, similar drug manufacturers can not obtain information about the original research and development of drugs.
  3. Last week
  4. Carbon emissions are a significant threat because they contribute to climate change. Climate change causes rising sea levels, extreme weather, and other problems that are currently facing our society. Many governments recognize this impact and are combating carbon emissions as a result. Here are just a few ways that world governments are taking a stand to reduce global emissions. The Paris Agreement This landmark decision was organized by the United Nations. It came into effect in December 2015. Simply put, this was a decision to hold governments responsible for reducing climate change. The goal is to keep the global temperature from rising to 2 degrees Celsius (35 degrees Farenheit) during this century. Ideally, it would even be below 1.5 Celsius (34 degrees Farenheit). This would be achieved through pooling together resources and improving technology to reduce industrial emissions. The Agreement will be revisited and updated every 5 years. While the United States has since pulled out of the agreement, other countries continue to stay in and work hard to lower their emissions for the safety of the planet. Carbon Taxes A carbon tax brings climate change responsibility closer to home. Carbon tax benefits include involving ordinary citizens in the effort against global warming. Each citizen (and, on a broader scale, industry) would be taxed according to the amount of carbon they produce on a regular basis. New York City is getting in on the game by imposing a "congestion pricing" plan. Taxi rates would go up the longer they sit in traffic. The money would then be returned equally among citizens through dividends, meaning that those who produced the least amount of carbon emissions would profit the greatest in the end. While there are concerns on how this would affect lower-income demographics, those working on the plan continue to change their approach to better suit the needs of modern citizens. Rewards for Clean Energy Efforts This financial benefit goes hand-in-hand with carbon taxes. In the United States, as well as other westernized countries, businesses can offset their carbon emissions by purchasing clean energy credits. Incentives include greater reliance on solar energy or wind power. Many rewards can come down on the local level as well. Some states provide tax reductions for installing solar panels. People who use solar panels can "sell" the electricity they generate back to the grid. Doing this gives profit to those individuals and companies who invest in renewable energy sources and works as a strong incentive toward more responsible business practices. Public Transportation Initiatives Not all cities are well known for having a good public transportation infrastructure. There are a few that are working to change that. For example, Indianapolis has instituted their Red Line Bus Service. It is a rapid-transit line that runs entirely on electricity. Other initiatives include making Denver, Colorado, a more walkable city by putting in parks. The city also wants to ensure a majority of residents live closer to public transportation in order to cut down on automobile emissions. Individuals can support their governments in these efforts as well. Installing solar panels in your home and using carbon calculators are great ways to inspire grassroots-level change. Recycling and supporting environmentally-conscious companies can also be a major step in the right direction. Climate change affects us all and it's important to get involved in whatever way we can.
  5. Tumors are high-risk and high-mortality diseases that pose a serious threat to human health. A large number of studies and prevention data confirm that early diagnosis and early treatment are the most effective ways to prevent and treat cancer and reduce mortality. Therefore, the search for cancer markers that can be used for early diagnosis has become the focus of attention. However, in addition to poor differentiation, easy metastasis and high-speed proliferation, malignant tumor cells are completely equivalent to normal cells in cytological behavior. No specific expression products or shedding components have been found so far, or various malignant cancer markers have not yet been discovered. This brings problems to tumor diagnosis and immunotherapy.The ideal specific cancer markers must meet the following requirements: (1) unique to a certain tumor; (2) related to tumor size and stage; (3) therapeutic monitoring; (4) prognosis; (5) Does not intersect with healthy people and other diseases. Cancer markers that meet these criteria have not been discovered so far and may never be found. In recent years, all cancer markers used in clinical practice are mostly tumor-associated antigens, or some normal people also have trace amounts, but the amount is different. In any case, finding tumor-specific antigens is still a hot spot for cancer research because of the refractory tumors and the need for biotherapy. Classification of common cancer markers: 1. Cancer Antigen 19-9 (CA19-9) The carbohydrate antigen CA19-9 is a monoclonal antibody numbered 1116NS19-9 obtained by Koprowski et al. in 1979 using a human colon cancer cell line to immunize BALB/c pure mice and hybridize with myeloma. A class of tumor-associated carbohydrate antigens, the antigen recognized by the monoclonal antibody is named the carbohydrate antigen CA19-9. CA19-9 is a tumor-associated antigen, which is related to Lewis blood group components and can be present on normal tissue cells. It is not unique to tumor cells. It is mainly found in epithelial cells such as the stomach, intestine and pancreas of the fetus. The biliary cells and the stomach, colon, endometrium and salivary gland epithelium can also be synthesized. In certain malignant tumors, CA19-9 in body fluids is often at a high level. Observing the changes of CA19-9 in vivo is conducive to early detection of the above-mentioned malignant tumors of organs, and has certain differential significance for the benign and malignant tumors. CA19-9 is detectable in serum, tumors, non-neoplastic diseases, and normal humans, but there are significant differences in CA19-9 levels in benign and malignant diseases. In benign diseases, normal people, serum CA19-9 elevation is usually low or transient, mostly below 100U/ml.In malignant tumors, the detection rate of different organs is different. At present, the increase of serum CA19-9 is more common in digestive tract tumors, especially pancreatic tumors, followed by biliary tract, colon, liver and stomach. In lung cancer, breast cancer and ovarian cancer. There is also a certain detection rate. The concentration of CA19-9 and the positive detection rate in the same organ tumor are related to the pathological type. For example, the CA19-9 concentration of colorectal cancer is higher in adenocarcinoma, mucinous carcinoma and signet ring cell carcinoma, but in papillary gland. Cancer and phosphorus cancer are lower. There are many clinical reports on the sensitivity and specificity of serum CA19-9 in various tumors, which are different from the disease and the number of cases in the selected cases, but the general trend is consistent. In the pancreatic cancer, the detection rate of serum CA19-9 is the highest. The sensitivity of each family is about 79%, even as high as 90.2%, and the specificity is between 70% and 90%. It has been used as a test for pancreatic cancer. Preferred serological indicators. The sensitivity in cholangiocarcinoma, gastric cancer, colon cancer, and liver cancer was 67% to 86%, 31.5% to 68%, 50%, and 49% to 60.9%, respectively. The sensitivity in lung cancer and breast cancer is low, about 10%. Many studies have shown that the concentration of CA19-9 is related to tumor size, especially in pancreatic cancer and colon cancer. A large number of studies have shown that preoperative detection of CA19-9 levels can help to determine the prognosis of patients with cancer, especially for patients with pancreatic cancer, colon cancer, hepatobiliary tumors, and gastric cancer. Preoperative high CA19-9 is a prognostic factor. The chances of recurrence and metastasis are high and the survival time is often short. The tumor marker CA19-9 is a tumor-associated antigen. This index has important significance in the diagnosis, curative effect, prognosis and postoperative monitoring of malignant tumors such as pancreatic cancer, cholangiocarcinoma, liver cancer, gastric cancer and colon cancer. However, its specificity is still low, and the detection rate varies from place to place. How to improve the clinical value of this marker remains to be further studied. The detection rate of CA19-9 varies from one report to another, and it is related to the selected method and the sensitivity of the selected kit, in addition to the difference in the condition and number of cases in the selected case. With the deepening of research, the emergence of more sensitive, more reliable, more reproducible, more convenient, more environmentally friendly and economical assays, the development of highly specific CA19-9 antibody will increase the value in tumor diagnosis. 2.Cancer Antigen 125 (CA 125) CA125 is a heterogeneous high molecular weight mucin-like glycoprotein containing mainly galactose, N-acetylglucosamine and N-acetylaminogalactose chains. The protein is partially rich in serine and can be recognized as an antigen by the monoclonal antibody OC125, hence the name CA125. Although the CA125 antigen is a glycoprotein, it has both membrane-bound and episomal states. CA125 in plasma and body fluids binds to glycoproteins of different relative molecular masses, respectively, and has the smallest subunit of CA125 immunoreactivity. CA125 is present in the body cavity epithelial cells of embryonic development and disappears several hours after birth, but reappears in ovarian cancer cells. Immunohistochemistry revealed that CA125 was found in fetal digestive tract epithelial cells, amnion, adult pleura, peritoneal mesothelial cells, fallopian tube endothelium, uterus and cervix, but no CA125 was found in adult and fetal ovarian epithelial cells. Under normal circumstances, CA125 does not enter the blood circulation, so the quality of CA125 is very low in healthy people and most benign diseases. CA125 can enter the blood circulation and various body fluids and exhibit high expression during the growth and metastasis of malignant tumors and when some non-tumor diseases progress. Elevated serum CA125 marker is a direct contact between the shed tumor cells and the systemic circulation when the "natural barrier" in the human body is destroyed, resulting in elevated serum CA125 levels. If the tumor is confined, CA125 has not yet reached the systemic circulation, and the level of CA125 in the blood is not high. Serum CA125 has been widely used in ovarian cancer screening, diagnosis, disease monitoring, prognosis and treatment. Serum CA125 combined with a variety of tumor markers can greatly improve the diagnosis and differential diagnosis of ovarian cancer. The half-life of CA125 used during chemotherapy can better predict the patient's response to treatment and monitor disease. The quality of serum CA125 can predict the trend of the subject to develop ovarian cancer. Serum CA125 detection combined with CT for the follow-up examination of patients with ovarian epithelial cancer is more valuable for detecting tumor recurrence. In addition, the current experimental and clinical studies on the treatment of ovarian cancer with CA125 monoclonal antibody have made great progress, and may bring new hope for the treatment of ovarian cancer. Examining the test results of elevated serum CA125 to patients can greatly improve the rate of return visits and improve the enthusiasm of women for regular gynaecological examinations. 3. Cancer Antigen 27.29 Breast carcinoma-associated antigen CA27.29 is a glycoprotein antigen produced by the MUC-1 gene. The product of the MUC-1 gene is MUC-1, which is a transmembrane glycoprotein expressed by glandular epithelia. The function of MUC-1 is associated with anti-pathogens and cell signaling. While overexpressed MUC-1, glycosylation changes, and abnormally intracellular localization have been related to cancers. Besides, MUC-1 was found in many types of malignant cells such as breast, ovarian, pancreatic, lung and prostate carcinomas. It can be shed into the circulation of the patients who have breast cancer. Hence CA27-29 is a part of MUC-1 and it can be detected by specific antibodies. Alterations in glycosylation of MUC-1 have great influence on its physiological and pathophysiological activity by affecting the interaction between the MUC-1 and other target proteins. It has been reported that the abnormal glycosylation of MUC-1 induces novel protein-protein interaction and increases the expression of phospho-IκB kinase (IKK)-β and phospho-inhibitor of nuclear factor kappa-B (IκB)-α which are the membranes of NF-κB family. By stimulation with inflammatory factors such as TNF-α, the cancer form MUC-1 induces activation of NF-κB members and interact with phopsho-p65, then moves to the nucleus to regulate the production of pro-inflammatory factors such as IL-6 and TNF-α. Then, the inflammatory cells like myeloid cells and neutrophils are recruited to the tumor site by the inflammatory cytokines. Moreover, the inflammatory cells are capable of enhancing tumor growth and progression by producing pro-inflammatory and pro-tumorigenic cytokines. For patients with breast cancer and ovarian cancer metastasis, especially those who have no clinical symptoms after treatment, when the serum CA27.29 is checked regularly, it is found that patients with CA27.29 measured value greater than 40 U/mL are less than the measured value. Patients with 40 U/m L or 40 U/m L have a much lower survival rate. Serum C A27.29 levels can also be used as a predictor of cancer recurrence in other adenocarcinomas, such as metastatic colorectal cancer and pancreatic cancer patients, and tumor metastasis can be found significantly earlier than other imaging techniques. This method is of little significance for the diagnosis and diagnosis of breast cancer patients during the construction period. In addition, in some diseases or physiological conditions, such as benign tumors, serum CA 27.29 values may also increase in the first 3 months of pregnancy, so attention should be paid to differential diagnosis. 4. Cyclin D3 (CCND 3) Encoded by CCND3 gene, CCND3 protein belongs to the highly conserved cyclin family. All the cyclin members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins act as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns. Different expressions contribute to the temporal coordination of each mitotic event. CCND3 forms a complex with CDK4 or CDK6, and functions as a regulatory subunit of those two proteins. A number of reports have revealed that CCND3 are involved in the phosphorylation of tumor suppressor protein Rb. The CDK4 activity associated with CCND3 was reported to be necessary for cell cycle progression through G2 phase into mitosis after UV radiation. Several transcript variants of CCND3 have been found so far. CDKs promote cell cycle transitions in mammalian cells by phosphorylating key substrates cyclins. Abnormal expression of cyclins was reported to be involved in many cancers progression. Highly expression of Cyclin D3 was reported in a number of tumor cells. Cyclin D3 gene is amplified in bladder carcinoma in situ. Genomic changes disrupting the expression of Cyclin D3 are involved in the aberrant growth of several human B-lymphoid malignancies. Targeting Cyclin D3 by miR-138 induces cell cycle arrest in hepatocellular carcinoma. Furthermore, Cyclin D3 is selectively required for proliferative expansion of germinal center B cells. For breast cancer, CCND3 is overexpressed in human breast cancer cell lines and primary invasive breast cancers. In addition, E1AF promotes breast cancer cell cycle progression via upregulation of CCND3 transcription. All the studies reveal that CCND3 is the marker of many tumor cells. Research and development of highly specific CCND3 antibody widely used in disease screening and therapeutic monitoring, providing key products to the research market and providing the highest value for the diagnosis and prognosis of many tumor cells Reference [1] Ni X G, Bai X F, Mao Y L, et al. The clinical value of serum CEA, CA19-9, and CA242 in the diagnosis and prognosis of pancreatic cancer [J]. Eur J Surg Oncol, 2005, 31(2):164-169. [2] Gorp T V, Cadron I, Despierre E, et al. HE4 and CA125 as a diagnostic test in ovarian cancer: prospective validation of the Risk of Ovarian Malignancy Algorithm[J]. 2011. [3] Cen P, Duvic M P, Kurzrock R. Increased cancer antigen 27.29 (CA27.29) level in patients with mycosis fungoides[J]. Journal of the American Academy of Dermatology, 2008, 58(3):382-386. [4] Büschges R, Weber R G, Actor B, et al. Amplification and expression of cyclin D genes (CCND1, CCND2 and CCND3) in human malignant gliomas.[J]. Brain Pathology, 2010, 9(3):435-442. [5] Zheng G, Patolsky F, Yi C, et al. Multiplexed electrical detection of cancer markers with nanowire sensor arrays[J]. Nature Biotechnology, 2005, 23(10):1294.
  6. Simple Introduction First of all, let’s start with its definition: Peptide mapping is the main method for the analysis and identification of protein products and preparations. In addition, there are some other core techniques such as peptide mass mapping and peptide mapping ms. The following are functions of Peptide mapping: To confirm that a protein primary structure (amino acid sequence) including the N and C terminals. To provide protein loci and the proportion of modified groups, such as glycosylation, acetylation, sulphates a00nd phosphorylation. To provide qualitative and quantitative information on protein degradation products To get information on protein oxidation and deamination directly. According to these useful features above, peptide mapping has already gained in popularity in biological field. After getting numerous data from peptide mapping, the next step is deeper analysis. A sample graph of peptide mapping Peptide Mapping Analysis Based on graphs of peptide mapping and also peptide mass mapping, scientists can get a lot of useful information. According to the size of molecular weight of proteins, peptides and amino acid composition characteristics, the use of strong specificity of proteolytic enzyme [is commonly endopeptidase] on the special peptide chain site will peptide fragment into smaller fragments, through the separation of a certain form characteristic fingerprint detection methods. eolytic enzyme [is commonly endopeptidase] on the special peptide chain site will peptide fragment into smaller fragments, through th The picture below shows the steps of peptide mapping method: Step 1: Protein digestion: Immobilized trypsin provides rapid and simple protein digestion with high reproducibility, high sensitivity and excellent data quality in a format that is compatible with automated operations. Step 2: Peptide separation: this technique provides a complete set of chromatographic tools for all development applications requiring peptide separation and analysis Step 3: Biological mass spectrometer: It provides a fast and easy to solve multicomponent analysis method, Used for sequence determination, structural analysis, molecular weight determination and component content determination of polypeptides. What’s more, it has the characteristics of high sensitivity, strong selectivity and good accuracy. Step 4: Peptide analysis software: Integrated software can save time and identify more materials. Simple software workflows can guide biotherapy, characterization pathways, and provide comprehensive coverage, including peptide sequence validation and identification of all variants and modifications. So peptide mapping analysis is quite effective and important in some specific aspect of research. Let’s take an example here: Study on quality control of impurities and harmful substances in Genetic Recombinant Drug is a crucial project., in particular, when the recombinants are used in the production of genetically engineered drugs undergo mutations. Probably, they would bring some mutations into drugs. Besides strengthen control of original material and process of production, peptide mapping analysis is necessary method to ensure safety and consistency. As a result, peptide mapping analysis has given rise to a number of new things. For instance, HPCE, A new electrical technology for separation which emerged in 1980s. Because of its relatively high resolution, HPCE has started a wider road for structural analysis and quality control of protein drugs. At present, in addition to the routine analysis of amino acid sequence of some small peptides, the peptide graph analysis is one of the important conventional indicators to control the consistency of most gene engineering products. All in all, technologies on peptide mapping have already penetrated into every corner of our everyday life.
  7. We all know the pressures of living green that have been thrown on our society for the last couple of decades. While we know it’s great for us, it’s not always great for our wallet. Things like installing solar panels are very costly to do. However, there are many green living practices you can do that can help pad your wallet instead of empty it. Get Rid of Old Scrap Metal There are scrap metal buyers literally everywhere across the country. Many will come to your doorstep and load up your old scrap metal for you. They’ll even pay you for the metal that they collect. While you may not be hoarding tons of scrap metal, small quantities can bring you some good money. Think about old appliances, piping, and other metal that you may have which accumulated over the years. Round it all up and give a scrap buyer a call to cash in on your old junk. Install Aerators for Low-Flow Water Sources Do you realize how much water you use on a daily basis? The United States Geological Survey Agency’s research shows that the average American uses 80 to 100 gallons of water per day. Do a little math for an entire month’s worth of water use and you’ll understand why your water bill is so much. You can help to curb the amount of water you use by installing water aerators and low-flow systems. For example, a water aerator in your sink will put in extra oxygen when you run the sink to help reduce the amount of water flow. In addition, low-flow showerheads can easily reduce the amount of water coming out of the showerhead while you’re enjoying a bath. Line Dry Your Clothes We all need to have dry, clean clothes each day. Running your dryer requires constant use of electricity for about 45 minutes to 1 hour depending on the size of the load and its materials. You can save running your dryer by simply hanging up your clothes outside. Clotheslines have been used by society for ages. They use the natural elements, like the wind and the sun, that wick away the water from your clothes. Going green is a revolution that requires a lot of small habits done consistently over time. You can do your part in going green by selling old scrap metal, installing water aerators, and line drying your clothes. All of these options will not only help the green initiative but they will also end up putting more money back into your wallet.
  8. What is an autoantibody? Autoantibodies are antibodies that target tissues, organs, cells, and cellular components. The growth, development and survival of the human body have the maintenance of a complete autoimmune tolerance mechanism. The normal immune response has a protective defense effect, that is, it does not react to its own tissues and components. Once the integrity of self-tolerance is destroyed, the body regards its own tissues and components as "foreign substances", and an autoimmune reaction occurs to produce autoantibodies. Normal human blood may have low titers of autoantibodies, but no disease occurs. However, if the titer of autoantibodies exceeds a certain level, it may cause damage to the body and induce disease. There are many kinds of autoimmune diseases antibodies , the most important of which are antinuclear antibodies. In addition, anticardiolipin antibodies, neutrophil cytoplasmic antibodies, anti-mitochondrial antibodies, anti-erythrocyte antibodies, anti-platelet antibodies, anti-endothelial cells antibodies, anti-neurovirus antibodies, rheumatoid factor, anti-thyroglobulin antibodies, anti-insulin bodies Antibodies and the like are also autoantibodies. Reasons for autoantibody production: Antibodies are generally produced by the immune system by foreign proteins or other substances (especially pathogenic bacteria) that enter the body and are used in immune reactions to eliminate harmful foreign substances. Usually, the immune system can recognize and ignore the body's own cells, and does not produce antibodies to it; at the same time, the immune system does not overreact to substances (such as food) that are not threatened in the environment. However, under certain circumstances, the immune system recognizes the body's own substances and treats them as foreign invaders, thereby producing antibodies (ie, autoantibodies) against these substances, triggering autoimmunity. These autoantibodies attack the cells, tissues, and organs of the body, causing an inflammatory reaction and causing damage to the body. The production of autoantibodies may be due to the presence of some of the same molecular structures between pathogenic antigens (bacteria, viruses, etc.) and their own components: an immune response that cross-reacts with autoantigens; or some infectious agents that cause autoantigens Denatured, the immune system produces autoantibodies to these exposed new antigens. The pathogenic effect of autoantibodies is still unclear. Whether it is the "cause" or "consequence" of autoimmune diseases has different opinions. For patients with high titers of autoantibodies, those without clinical symptoms may not need treatment, but should go to the hospital regularly. Review and review. In tumors, inflammation, autoimmune diseases (such as lupus erythematosus, genital warts, Crohn's disease, multiple sclerosis), neurodegenerative diseases, infectious diseases, etc., a large number of autoantibodies are produced and accumulated in patients. Some autoantibodies have emerged in the early stages of a specific disease, even before the onset of symptoms of the disease, providing a reliable disease biomarker for the early diagnosis; some autoantibodies are the body's own protection against disease. Sexual antibodies, which provide new ideas for the treatment of the disease, as data from the world-renowned pharmaceutical giants show that 60% of the profits of large pharmaceutical companies have come from drugs that belong to antibodies. So how do you discover these potential autoantibodies? Methods for screening for autoantibodies: At present, the most suitable method for screening autoantibodies is the protein chip method. A protein chip often has thousands of protein spots, which can screen one autoantibody that can interact with these proteins at one time, and then pass fluorescent These autoantibodies can be found by incubation of the marker against the anti-Human IgG secondary antibody and fluorescence detection. The principle is simple, but it is very difficult to do, why? This has to say about the binding process of antibodies to antigens. In short, the corresponding antibody recognizes a specific epitope on the antigen and then binds it. The epitopes are divided into two types, linear epitopes and non-continuous epitopes. A linear epitope consists of a contiguous sequence of amino acids. An antibody that recognizes a linear epitope recognizes this amino acid sequence and produces an antigen-antibody binding reaction; a non-contiguous epitope is composed of a discontinuous amino acid, which is correct by the antigenic protein. After folding, they are close together and recognized by the corresponding antibody, producing an antigen-antibody binding reaction. In the body, most autoantibodies are non-continuous epitopes that recognize antigens. Correct identification and screening of these autoantibodies requires that the proteins on the protein chip be full-length, correctly folded, and biologically functional. However, the traditional protein chip can only guarantee that the protein synthesized on the chip is full-length (some can not be guaranteed), can not guarantee the correct folding of the protein, and can not guarantee the normal biological function of the corresponding protein. Other problems affecting the screening of autoantibodies by traditional protein chips include high CV values (>30%), poor reproducibility, low resolution, high background signal, and inability to distinguish autoantibodies with low expression levels. Screening for autoantibodies with such protein chips is like fishing with a large network full of loopholes. Screening of autoantibodies with such protein chips has brought great resistance to researchers and companies in the research of antibody screen. Sengenics' ImmunomeTM Protein Chip Research Platform, invented by Professor Jonathan Blackburn at the University of Cambridge in 1996, is a collaboration between Oxford and Cambridge. It is the only one in the world that is fully-length, correctly folded and functionally validated. Protein chip platform. Autoantibodies that recognize non-contiguous epitopes can be screened for advantages that cannot be replaced by other protein chip products. The ImmunomeTM Protein Microarray Research Platform contains 1631 full-length, correctly folded and functionally validated human proteins, covering cancer antigens, transcription factors, kinases, signaling pathway molecules, etc., to meet the research needs of users in different directions. Daban's low autoantibodies provide strong technical support as biomarkers. Compared to traditional protein chip products in the screening of autoantibody applications, Sengenics ImmunomeTM protein chip products can be described as "Skynet is restored, not leaking", full-length, correct folding, functional verification, wide coverage, low coverage CV low background signal, high-resolution full-generation protein chip platform technology helps researchers and business users to "capture big fish" in the field of autoantibody research, and return home.
  9. Earlier
  10. Everyone says that the grass is greener on the other side of the fence, but green doesn’t always mean environmentally friendly. Those homeowners who want to be conscious of their impact on the environment can start with their own yard care practices and what they grow. Doing so can ensure that both your yard and the natural landscape beyond stay green and healthy, and here are a few ways you can accomplish that. Use Native Plants When you use plant life that is common to the community, it helps provide food and resources for native animals. You can ensure local species survive with trees, shrubs, and plants that offer food and nesting material. Growing native plants also prevents the spread of aggressive foreign plants that could overtake the local native plants in your area. Plus, local plants are easier to grow and care for because they thrive in your climate. If you want a low-maintenance yard, then the garden center can show you which plants are easiest to care for and hardy plants for your climate. Feed Pollinators Bees help pollinate crops and flowers. Martha Stewart says 80 million pounds of pesticides are put on crops and communities across the United States annually. These chemicals kill bees and other animals that are susceptible to small environmental changes and displace others. Something as simple as planting flowers and fruits to provide nectars for pollinators can do a great deal of good in giving your local bees, butterflies, hummingbirds, and other pollinators a place to refuel. Anything that flowers can work, so when you’re considering plants to grow in your yard and garden, keep that in mind. Plant Trees You can help the environment by planting trees. Not only do trees help clean the air, but they also offer valuable shelter to birds and animals. Fruit trees especially can be a source of nourishment for the local wildlife. Not only do the flower buds provide nectar for pollinators, as previously mentioned, but they also give fruits and seeds to birds, squirrels, and other animals that are now running out of healthy food sources and shelter. To encourage birds to return to your yard, planting oak trees for shelter is a great idea, and the acorns they grow make for great food for animals. Cardinals and bluebirds are partial to dogwood trees, and pine trees are excellent for most bird species, as well as for animals. Use Organic Fertilizers Another tip is to work with gardening centers and landscaping companies that offer organic fertilizers as opposed to the more toxic varieties. These organic fertilizers are safe for pets and any birds, bees, or animals that visit your yard while still creating a green lawn. If you want to attract specific species, then the landscaper can also give you ideas about what bushes or flowers you can plant to attract them to your yard. Make sure that the fertilizers you get work well with your intended plants and lawn, as different plants and regions require different nutrients to thrive properly. You can make sure your side of the fence is greenest by adding local plants and trees. Organic fertilizer will protect your pets and ensure bees and birds are safe on your property. Whether you are familiar with the area or you want to know more about specific plants, the local garden center or landscape provider can help you discover the right ways to help the Earth in your little corner of the world.
  11. Your home’s features and condition play a major role on the impact you make on the planet. Many people assume that they need to make huge, expensive home improvements to create a green living environment. While installing solar panels and a rainwater collection and purification system are some of the many expensive projects that you could invest in, proper home maintenance can have a beneficial impact as well. These are some of the maintenance tasks to complete regularly to create a greener home environment. Schedule HVAC Service Regularly Living without an HVAC service would be miserable for most people. While this system understandably uses a significant amount of energy, it may currently be using more than it needs to. For example, when the system is dirty or developing signs of damage, the equipment may run more frequently or for longer periods of time than it otherwise would. This directly wastes energy and creates pollution in the process. When you schedule regular HVAC maintenance service, the components will be clean so that the system can work efficiently. In addition, developing repair issues can be identified and addressed quickly before they become major issues. Maintain Your Plumbing Features Fresh water is in short supply, so water conservation is a primary concern. In some homes, hidden water leaks waste tons of water before they are identified and repaired. In other homes, a huge leak spews hundreds of gallons of water or more into the home in a very short period of time. While not all leaks can be prevented, you can take steps to prevent some of these issues. For example, you can reduce your water pressure to minimize strain on the pipes. You can also invest in a water softener and reinforce pipe joints. Re-Seal Doors and Windows Periodically Energy loss also occurs through damaged window and door seals. These seals tend to deteriorate rapidly, and they may need to be replaced at least once per year. By doing so, you can keep climate-controlled air in the home and help your HVAC system to work more efficiently. You may also consider installing solar film over your windows for additional benefit. Each of these maintenance tasks should be included in your regular home care schedule. However, it is easy to overlook or delay working on them. Now that you know that they affect your property’s condition as well as your impact on the environment, you can see that these tasks deserve your regular attention.
  12. Whenever there is the talk of switching to residential solar panels, most of the rules are as follows: If the consumer can also add solar during access to grid electricity, then, in reality, he will not pay much attention to an angle, unless the solar system is completely prohibited and does not provide funding. Because, after paying the solar energy system first, they get the benefit of free energy. So we start paying attention to saving on our electricity bill. Depending on the cost of the system, the same is done as a fixed period of time to save the payment. That time depends on the initial cost and any funding cost, maintenance costs and consumer's energy. If we believe in most cases, the cost of solar water or the Hitter P.V system is recovered in 6-10 years. If any kind of government incentive (credit tax) is available then the normal work becomes small. A solar system can increases the prices of the houses, so the consumer is encouraged to also contribute to a clean environment. Consumers using solar water have received more profits. If any member of the family takes a bath for a long time, then he does not wait for the water to heat until others take a shower. The main reason for this is that we have solar heater water at home, which has been around us since 1979. This solar system is ambitious. Their situation is slightly different from the power provider's point of view. This is the only support for them that a solar system produces more energy during its regular time. Which can be specially provided by less efficient equipment, or they do not have to invest in additional ways only to cover the peak load. Although it is for their side, that there are many residential customers for the party who have PV and PD about 20% more than their load. So this can introduce the instability of the grid, but if the energy reserves are introduced to consumers and energy providers, then it reduces the maximum. What should be included in the total cost or cost of a solar panel system for your own home if you have more providers from other providers and equipment? 1. Warranties of solar panels and solar inverter from manufacturers are usually up to 25 years. 2. If you want to secure solar panels on your roof, then racking and mounting for them. 3. Fixes for more power equipment such as cable laying grooves, junction boxes, etc. such as installation. 4. Construction of approvals from the areas according to their rights, including inspection form after installation of a permit method and installation of the solar system. 5. To get approval through its utility and to create a pure metering agreement with the company during its utility, there is also a usefulness inspection on the basis of where you are located. 6. Solar installation with a warranty usually with the company of the Solar System, only the solar installer works from 5 to 10 years. 7. The rest of the work is also established with the installation of solar panels or panels, inverters and solar panels by qualified electrical contractors. 8. To avoid a zero-down system for the debt system, including the option to cover the cost of a solar system, the federal tax credit portion, unless you do not do for the next year's taxes. This analysis shows that after installing the system you are likely to get the utility bills, it is likely that utility bills are low
  13. The amount of plastic that’s being discarded on a daily basis is staggering. Much of this plastic is ending up in the oceans and presents a crisis to these sensitive ecosystems. Here are some of the ways that companies are working to reduce the amount of plastics that are entering the environment. Tackle Recycling Initiatives Many of the single use plastic containers can be eliminated simply by investing in recycling efforts. Some cities are moving to ban the use of plastic bags in an effort to help save the environment. The recycling efforts don’t stop with just plastic bags, but can be realized in other areas. You can help by investing in reusable coffee cups, reusable lunch containers, and other reusable items that are being made by these environmentally conscious companies. Invest in Removal Recycling alone isn’t going to protect the oceans. This is because of the amount of plastics that already exist within the environment. Removing these harmful products from the oceans is the only solution when it comes to cleaning them up. Some companies, such as bionicyarn.com, recover plastic waste from the oceans in order to make new products can show you the ways that some businesses are embracing the concept of using trash as their business model. Develop New Technologies Even with all of these efforts being put into place, it won’t be enough to reduce the amount of plastics that are available. This means that new technologies need to be developed in order to create plastic-like substances that are biodegradable in nature. You may have heard about companies that are looking into using corn-based derivatives in order to create packaging for their products. New technologies such as this can work towards the goal of eliminating the amount of plastic that has a chance to enter the oceans. Awareness Efforts Companies that make the leap to more recycled choices, such as having you return their packaging for reuse, is one way that awareness efforts can benefit the oceans. You can do your part by purchasing from these companies so that you can voice your opinion in an economic manner. Other companies are more likely to jump on the bandwagon if they see that this is the type of technology that consumers like yourself want to invest in for the future. Big business needs to come up with solutions that will help to eliminate this environmental crisis. Consider these ways when it comes to how companies making trash their business is the right solution.
  14. These days more and more people think about the advantages that they can experience when they decide to go off the grid and make full use of solar panels for their home. This is a smart decision to make, the thing you need to understand is that you need to know the components that make up these systems. This will be useful information that will help you when you need it the most in the process of building your own system or when you are in need of having to make much-needed replacements to parts that have failed. So let’s dive into this subject and show you the things that you need to seriously think about when it comes to solar power components. The first thing that needs to be addressed quickly is the fact that you will want to think about going basic with the setup that you are doing. This is important in the fact that you can go with a basic setup and save a good amount of money and get a good return on your initial investment. The first component of these systems is that of the panels themselves. This will be the biggest cost that you will have to fork over out of pocket. It is important that you take note of the placement of your panels like these will make a big difference in the quality of performance that you will get from your panels and will determine exactly how well that these operate on the whole. The next thing is the mounting equipment that you will use to mount your panels. This has a duel edge sword to it as you will need to be aware of the placement of this first for the fact that you will want to get the best benefit from these over the course of a year or so. In addition to this, you will want to keep an eye on this as you will need to have these mounted for at least 25 years or more. Inverters are the things that take the solar energy and convert it into energy that you can use for your home. This is an element that can break easily so it is best to always go with a quality product when you can. The tracking mounts are another element that is crucial as these allow the panels to adjust throughout the day to ensure that you are getting the most exposure from the sun. make sure that you take some time to buy the ones that will move bilaterally as this will give you the best overall results for your solar panel efforts. The last components are that of the electrical. You will want to make sure that you have installed disconnect switches, meters and wiring to help and keep your system running the way that it should for the most part. A disconnect switch will be vital in helping you to be able to cut the power should something odd happen with your electrical system it will be vital that all the members of your family know where this is so that they can easily reach it and be able to kill the power to the system. As you can see the solar power components are very important to the operation of a system that you will be able to get the most out of. Not letting this subject get to you, will be vital in helping to create a money saving opportunity.
  15. While trying to be more environmentally friendly is a commendable goal, a lot of people are wary of making the lifestyle changes it requires. One of the more prominent concerns that people have is the cost required to “go green.” As it turns out, not only can it be affordable to go green, but you can actually profit off of many of the efforts involved. Here are just a few ways that anyone can cash in on environmentally friendly choices. Tax Incentives Any time you can write something off on your taxes, it is always a welcome surprise. However, did you know that by purchasing a solar panel system for generating energy for your home comes with a 30% tax credit that you can use as a tax write off? This federal tax incentive has been extended on through 2021. While you can really save on your taxes using this form of alternative energy, you must act before the end of 2021 to take advantage of this government tax break. Using solar energy can also save you money on your utility costs by supplying energy to your home that you don’t have to get through a service. While most people double up by purchasing energy alongside their solar panels, the panels themselves cut down on how much energy you need to buy elsewhere, and many companies will pay you for the excess energy that your solar panels generate. Trading Cash for Recycling If you have old appliances or scrap metal laying around, then you might be able to turn these items into cold hard cash. Most scrap metal services will pay you for any metal you can bring to them, including old radiators, appliances, electronics, and so on. While most wires can’t be directly recycled due to their rubber coating, there are places you can sell those, as well, where the rubber coating is stripped and recycled separately from the wire inside. Other recycling services will pay for cartons, recyclable plastic containers, and other materials depending on their specialty. Taking advantage of this is great for the planet and also gives you some extra spending money from what otherwise would just have been trash. Energy Savings Going green does more than just earn you cash, however. Eco-friendly lifestyles and behaviors also encourage you to be more efficient with the money that you already have. Replacing energy inefficient appliances, such as your dryer or HVAC system, with energy-efficient models can really help you keep more of your monthly income. This is because energy efficient appliances tend to use less electricity; thus, helping to keep your electric bill at a minimum. Most newer models have been upgraded to meet modern energy efficiency standards, but finding Energy Star rated appliances can take your energy savings one step further. Saving Water Whether you are doing laundry in a water-saving washing machine or flushing a water efficient toilet, the amount of water you save matters. While the earth is composed mostly of water, only less than 3-percent of this water is actually drinkable. The rest of the water is salt water and not suitable to use drinking. So, using water-efficient appliances cuts your water bill down and, at the same time, it helps out everyone else by preventing our planet’s drinking water from being used up to quickly. To take your water conservation a step further, you can invest in a greywater recycling plant that can be installed on your property to treat and reuse non-drinking water, or greywater, for your sprinklers, toilet, and other appliances. While many are wary of the costs of green living, it’s clear that there is more to be gained than lost from making those lifestyle changes. Whether earning cash from recycled items, getting tax incentives from renewable energy solutions, or saving money in utility costs, there are a lot of ways that anyone can gain from protecting the planet. Eco-responsible living is a benefit both to the planet and individuals, and should be highly considered by anyone who wants to live responsibly while making ends meet.
  16. Researchers from the University of North Carolina Lineberger Comprehensive Cancer Center have discovered how different mutations in a specific gene help drive glioblastoma, the most lethal form of brain cancer. In the preclinical study, researchers investigated whether the location of where the mutation occurred within the sequence of the PIK3CA gene affected the mutation's ability to help drive cancerous growth. They also tested whether mutations within certain sequences of the gene were linked to better responses to particular drugs. They found mutational status was not linked to a response to a single targeted drug, but it was to a combination of treatments. UNC Lineberger's C. Ryan Miller, MD, an associate professor in the UNC School of Medicine Departments of Pathology and Laboratory Medicine, Neurology, and Pharmacology, said the findings, published in the journal PLOS One, call for a more refined approach to precision medicine for glioblastoma, requiring more information about mutations that occur in a particular tumor. "One approach to personalized medicine has been to sequence the tumor to find any type of mutation in genes for which there are drugs that target them, and then treat all patients the same," Miller said. "We think it's going to need to be more nuanced than that. We will need to take into consideration not only whether there are mutations in genes like PIK3CA, but also: where the mutation is in the gene, and what is its biochemical mechanism? Not only that, but what are the other concurrent mutations in the tumor -- what other genes are mutated, and are they druggable too?" Glioblastoma is the most common primary malignant brain tumor in adults. Current treatments, which can include surgery, radiation and chemotherapy, have had limited effectiveness. A newly diagnosed patient has median survival of 12-15 months, and the five-year survival rate is less than 5 percent. Clinical trial results have been disappointing for drugs targeting certain molecular pathways driven by mutations commonly found in the disease. Studies have found that the PIK3CA gene is mutated in about 10 percent of glioblastoma cases. Unlike some cancers in which mutations frequently occur in a specific location, or "hotspot," of a gene, mutations in PIK3CA can occur in multiple different parts of the gene in glioblastoma. "For most of the successful examples of personalized medicine in solid tumors, the targets are hotspot mutations that activate a gene, which activates its signaling pathway, which drives the disease," Miller said. "Those tumors are addicted to that signaling. What interested us about this target is it didn't really fit that profile. The mutations were in multiple protein domains, and based on the sequence you could predict that they would have different biochemical mechanisms of action." In studies in glioblastoma cells, researchers found that specific mutations in the PIK3CA gene help to drive the cancer. And while the presence of mutations was not linked to a greater response to treatment with a single drug targeting the PIK3CA pathway, they did see improve response with two different therapies: buparlisib and selumetinib. "When we did the drug studies, we found that the mutation status of the cells really didn't predict response to the drug, unless we included a second drug in combination that targeted a parallel pathway," Miller said. The next step for the researchers will be to evaluate drugs targeting the particular downstream effects of the different pathways. Miller said researchers hope future studies could help identify additional potential therapeutic targets in glioblastoma, while helping to guide clinical trials using existing drugs. Individual authors were supported by the University Cancer Research Fund, the NationalCenter for Advancing Translational Sciences, the National Cancer Institute, the Robert H. Wagner Scholar, Bill Sykes Scholar in Pathobiology and Translational Science award, the UNC Graduate Training Program in Translational Medicine, and the National Institute of Environmental Health Sciences. In addition to Miller, the study's other authors are Robert S. McNeill, Emily E. Stroobant,Erin Smithberger, Demitra A. Canoutas, Madison K. Butler, Abigail K. Shelton, Shrey D. Patel, Juanita C. Limas, Kasey R. Skinner, Ryan E. Bash, and Ralf S. Schmid.
  17. Positional mutation is a protein engineering technique that substitutes, inserts or deletes specific nucleotides in known DNA sequences based on the known structure and function of proteins to produce mutant protein (enzyme) molecules with novel traits. The technology is widely used in the biological and medical fields. Position mutation technology has the characteristics of high mutation rate, simple and easy to perform, and good repeatability. As a research method, localization mutation technology is also widely used to study the relationship between protein structure and function, so as to elucidate the regulation mechanism of genes, the etiology and mechanism of diseases. Introduction The "small change" of protein molecules based on natural protein structure refers to the modification, substitution or deletion of a few residues of proteins of known structure. This is the most widely used method in protein engineering, and can be mainly divided into proteins. Two types of modification and gene location mutation. Gene-localized mutation refers to the transformation of protein molecules at the genetic level, that is, the method of site-directed mutagenesis, the insertion, deletion, substitution and reorganization of nucleotide codons of genes encoding proteins, and then the mutated genes are carried out. The protein expresses and analyzes the functional activity of the expressed protein, and the result provides a new design for protein molecular engineering. Design goals and solutions for location mutation The common design goals of localization mutations are to improve the heat and acid stability of proteins, increase activity, reduce side effects, improve specificity, and conduct structural-functional studies through protein engineering. Hartley is equal to 1986 to complete a design goal and solution that we want, and still has important reference value. The stability of protein is an important prerequisite for the normal biological activity of proteins. Therefore, improving the stability of proteins has become one of the important goals of protein design and transformation. Type of mutation There are many ways to change the nucleotide sequence of a gene, such as chemical synthesis of genes, direct modification of genes, and cassette mutation technology. Depending on the manner in which the gene is mutated, it can also be classified into three categories: insertion of one or more amino acid residues; deletion of one or more amino acid residues; replacement or substitution of one or more amino acid residues. In order to achieve the purpose of gene location mutation, in vitro recombinant DNA technology or PCR method is often used. Site-directed mutation The amino acids in a protein are determined by the triplet codon in the gene. By changing one or two bases, the amino acid species can be changed to produce a new protein. It is usually the amino acid that changes a position in the functional region to study the structure, stability or catalytic properties of the protein. The work of point mutation is the main body of current protein engineering research. So far, many kinds of proteins such as subtilisin, T4 lysozyme, dihydrofolate reductase, trypsin and ribonuclease have been modified. For example, replacing Asn117 of a tissue-type plasminogen activator (t-PA) with Glu117, thereby removing an original glycosylation site; since the original sugar chain can promote t -PA is cleared from plasma, so point mutations can reduce plasma clearance of t-PA and prolong plasma half-life. Box mutation In 1985, Wells proposed a genetic modification technique for a box-type mutation that can produce 20 different amino acid mutants at one site, and can perform "saturation" analysis of important amino acids in protein molecules. Using the localization mutation, two original vectors and endonuclease cleavage points not present on the gene are added on both sides of the amino acid code to be modified, and the endonuclease is used to digest the gene, and then the synthesized double-stranded DNA fragment with different changes is substituted for digestion. part. A variety of mutant genes can be obtained in such a single treatment. Procedure for locating mutations The protein molecular design program for gene localization mutation follows the procedure in the design principle, but the gene location mutation has its own particularity, and its specific procedure is as follows. Establish a structural model of the protein under study Establishing a three-dimensional structural model of a protein is critical to establishing a mutation site or region and predicting the structure and function of the mutated protein. The structure can be determined by X-ray crystallography, two-dimensional nuclear magnetic resonance, or the like, or a structural model can be established based on the structure of the analog or other structural prediction methods. Identify locations that have a significant impact on the required properties Predict the structure of the mutant Construct mutants. Mutant protein Examination of mutant proteins About us We provide custom protein services in the biological sciences, enabling access to the latest tools, techniques, and expertise with competitive pricing and rapid turnaround time. We serve a broad spectrum of industrial and academic clients with a commitment to delivering high-quality data and customer services. Here are some our products: SPR, Co-Immunoprecipitation, Pull-Downs, CLIP-seq, etc.
  18. Positional mutation is a protein engineering technique that substitutes, inserts or deletes specific nucleotides in known DNA sequences based on the known structure and function of proteins to produce mutant protein (enzyme) molecules with novel traits. The technology is widely used in the biological and medical fields. Position mutation technology has the characteristics of high mutation rate, simple and easy to perform, and good repeatability. As a research method, localization mutation technology is also widely used to study the relationship between protein structure and function, so as to elucidate the regulation mechanism of genes, the etiology and mechanism of diseases. Introduction The "small change" of protein molecules based on natural protein structure refers to the modification, substitution or deletion of a few residues of proteins of known structure. This is the most widely used method in protein engineering, and can be mainly divided into proteins. Two types of modification and gene location mutation. Gene-localized mutation refers to the transformation of protein molecules at the genetic level, that is, the method of site-directed mutagenesis, the insertion, deletion, substitution and reorganization of nucleotide codons of genes encoding proteins, and then the mutated genes are carried out. The protein expresses and analyzes the functional activity of the expressed protein, and the result provides a new design for protein molecular engineering. Design goals and solutions for location mutation The common design goals of localization mutations are to improve the heat and acid stability of proteins, increase activity, reduce side effects, improve specificity, and conduct structural-functional studies through protein engineering. Hartley is equal to 1986 to complete a design goal and solution that we want, and still has important reference value. The stability of protein is an important prerequisite for the normal biological activity of proteins. Therefore, improving the stability of proteins has become one of the important goals of protein design and transformation. Type of mutation There are many ways to change the nucleotide sequence of a gene, such as chemical synthesis of genes, direct modification of genes, and cassette mutation technology. Depending on the manner in which the gene is mutated, it can also be classified into three categories: insertion of one or more amino acid residues; deletion of one or more amino acid residues; replacement or substitution of one or more amino acid residues. In order to achieve the purpose of gene location mutation, in vitro recombinant DNA technology or PCR method is often used. Site-directed mutation The amino acids in a protein are determined by the triplet codon in the gene. By changing one or two bases, the amino acid species can be changed to produce a new protein. It is usually the amino acid that changes a position in the functional region to study the structure, stability or catalytic properties of the protein. The work of point mutation is the main body of current protein engineering research. So far, many kinds of proteins such as subtilisin, T4 lysozyme, dihydrofolate reductase, trypsin and ribonuclease have been modified. For example, replacing Asn117 of a tissue-type plasminogen activator (t-PA) with Glu117, thereby removing an original glycosylation site; since the original sugar chain can promote t -PA is cleared from plasma, so point mutations can reduce plasma clearance of t-PA and prolong plasma half-life. Box mutation In 1985, Wells proposed a genetic modification technique for a box-type mutation that can produce 20 different amino acid mutants at one site, and can perform "saturation" analysis of important amino acids in protein molecules. Using the localization mutation, two original vectors and endonuclease cleavage points not present on the gene are added on both sides of the amino acid code to be modified, and the endonuclease is used to digest the gene, and then the synthesized double-stranded DNA fragment with different changes is substituted for digestion. part. A variety of mutant genes can be obtained in such a single treatment. Procedure for locating mutations The protein molecular design program for gene localization mutation follows the procedure in the design principle, but the gene location mutation has its own particularity, and its specific procedure is as follows. Establish a structural model of the protein under study Establishing a three-dimensional structural model of a protein is critical to establishing a mutation site or region and predicting the structure and function of the mutated protein. The structure can be determined by X-ray crystallography, two-dimensional nuclear magnetic resonance, or the like, or a structural model can be established based on the structure of the analog or other structural prediction methods. Identify locations that have a significant impact on the required properties Predict the structure of the mutant Construct mutants. Mutant protein Examination of mutant proteins About us We provide custom protein services in the biological sciences, enabling access to the latest tools, techniques, and expertise with competitive pricing and rapid turnaround time. We serve a broad spectrum of industrial and academic clients with a commitment to delivering high-quality data and customer services. Here are some our products: SPR, Co-Immunoprecipitation, Pull-Downs, CLIP-seq, etc.
  19. The genetic engineering was established in the early 1970s and it has played an important role in the field of biology after decades of continuous progress and development. Plant genetic engineering technology uses recombinant DNA technology to systematically transform and recombine biological genes by artificial "shearing" and "splicing" in vitro, and then insert and integrate into the recipient plant genome to reorganize. The gene is expressed in the recipient cell, so that the recipient plant obtains a new shape and breeds a new variety with high yield, multi-resistance and high quality. The research and application of plant genetic engineering is flourishing around the world and is considered to be the hope of agriculture in the 21st century. It plays an important role in the new agricultural revolution. 1. Plant genetic engineering and its technologies Based on human's goals and design, plant genetic engineering was conducted through split, integrate, splice, etc. in vitro to make the genetic material is recombined, and those features are then transferred to the plant through a specific vector (such as plasmid, phage, virus, etc.) intracellularly, and the expression of the required genes are expressed in cells. With this, a new plant type is created. Genetic engineering has a superior development space for improving plant traits, quality, increasing yield, and improving plant resistance to diseases, insects, and stress resistance. Therefore, its future development is extremely broad. Plant engineering genetic technology has greatly expanded the gene pool available to plants, and it has become a reality to initiate directional mutation according to people's preset plans, which has brought huge changes in plant breeding (mainly in the following aspects: break reproductive isolation, making it creates conditions for broadening the available gene banks of plants, and providing new techniques for manipulating mutations; most of the genes used for genetic engineering breeding have been studied more clearly. The purpose of improving plants is clear, and the selection means is effective, so that it is possible to produce directional variation and directional selection; by improving some key traits of plants, the original promotion varieties will be improved to a large extent, not only can shorten the breeding period, but also make a comprehensive breakthrough in different ecological regions; with the deepening of understanding of genetic engineering, the cloning of new genes and the improvement of transgenic technology, and the targeted operation of multiple genes will also be possible, which is difficult to imagine in conventional breeding, and may lead to new "green" Revolution"). 2. The possible risk and mechanism of genetically engineered plants People have gradually realized that because the current level of science and technology can not accurately predict all the manifestations of plant genetic engineering, the safety of plant genetic engineering has attracted people's attention. 2.1. Possible risk of genetic engineering plants (1) The threat of genetically engineered plants to environmental safety: ①The effect of insect-resistant genetically engineered plants on other organisms. The insecticidal effect of insect-resistant genetically engineered plants is non-selective. It can also kill beneficial insects or other organisms in the environment while killing pests. Even when their residues are degraded in the soil, they will also affect insects or microorganisms in the soil. ②Antiviral genetically engineered plants pose a risk of new viruses. At present, in genetic engineering of antiviral plants, most of the genes introduced into plants are sequences derived from the viral genome, and the most widely used are CP gene, MP gene and replicase gene. ③The potential threat of genetically engineered plants to the Earth's ecosystem. After the release of genetically engineered plants, gene drift is inevitable, which causes the transferred genes to be passed on to other crops. Metabolites of genetically engineered plants will spread to the external environment, causing a chain reaction. (2) The harm of genetically engineered plants to human health: ①Genetically engineered plants may contain known or unknown toxins that are toxic to humans. ②Genetically engineered plants may contain known or unknown allergens, causing allergic reactions in the human body and even death. ③Genetically engineered plants produce certain nutrients or nutritional qualities that cause certain symptoms in the body. ④After the genetically engineered plant is eaten by humans, the food will pass the drug resistance gene to the pathogenic bacteria in the human body, which will make the body resistant. 2.2 The mechanism of genetic engineering plant to cause risk (1). Genetic engineering causes mutations in DNA in plants. Genetic engineering introduces foreign genes into plant gene tissues, causing DNA mutations in plants. Different locations of foreign gene introduction may lead to changes in plant gene expression, enzyme expression, or in unknown growth and metabolism in plants, which may produce or polymerize certain harmful substances, thereby threatening human health. (2). Genetic engineering causes plants to contain new proteins that directly or indirectly endanger human health. Plant genetic engineering introduces genetic information into plants, and this genetic information may come from any organism on the earth that allows plants to produce new proteins. This new protein may directly harm human health or this new protein affects plant cell metabolism and changes the nutrient composition of the plant, thereby affecting human health. (3). The harm may be caused by the unpredictability of genetic engineering. Although DNA can be spliced very accurately under laboratory conditions, the effect of a foreign gene into a plant on the entire plant genome cannot be fully predicted and controlled. The plant is an extremely complex living system, and our existing scientific knowledge and technical means cannot fully control the inheritance of plants. 3. Suggestions on improving the safety management of plant genetic engineering (1). Have a full understand on the strategic significance of genetic engineering safety management, and improve the safety awareness of genetic engineering of all people, especially leading cadres and related scientific research and staff, and popularize relevant laws and regulations on genetic engineering safety management. (2). Formulate a comprehensive "Genetic Engineering Law" to ensure that all laws and regulations on the safety management of genetic engineering are available. (3). Establish an effective and timely genetic engineering supervision and reporting system, and conduct long-term follow-up monitoring of projects with higher risk levels to ensure that genetic engineering safety is within the controllable range. (4). Establish a scientific genetic engineering risk assessment mechanism and explore the establishment of an authoritative genetic engineering risk assessment social organization. Strengthen the approval of research, development, promotion, import and export, and extend the review time of high-risk projects. With the rapid development of plant genetic engineering technology, the emergence of new gene introduction technology (such as CRISPR/CAS9, TALEN-Mediated DNA Insertion, Virus-induced Gene Silencing etc.)and the technology of crop tissue culture are more convenient and effective. In the near future, it is expected to produce high-yield, high-quality, high-efficiency, disease-resistant, insect-resistant and anti-adversity crops. A new crop variety with excellent traits will benefit human beings and become an important weapon for human beings to understand nature and transform nature. At the same time, when seeing the achievements of genetic engineering plant, we must also see the risk of genetically modified plants.
  20. Going green is a concept that we can all get on board with. However, it can seem difficult to know what practices to do other than your traditional recycling instead of throwing items in the trash. In today’s short article, we’re going to discuss some small eco-friendly changes you can make to your daily living that will have a large impact on the going green initiative. Use Ecological Home Services If you’re a homeowner, it’s likely that you use home service providers for various issues or improvements you want to make to your home. When considering who to hire, you should look into those who practice eco-friendly methods. For example, hire an ecological pest control service that only uses environmentally-friendly treatment methods. This can help to keep pesticides out of your home. It will also ensure that your family doesn’t have any negative reactions to harmful treatment pesticides that other home servicers use. Use Canvas Bags at the Grocery Store We’ve all seen those plastic grocery store bags blowing around in the wind as people tend to not dispose of these bags correctly. When you use canvas bags, you can help to cut done on the number of plastic grocery store bags being produced. In fact, the more people who bring their own canvas bags to the grocery store, the less plastic bags the store will order. These bags carry their own advantages as well. For example, they’re much sturdier than those plastic bags, which makes them great for carrying canned goods and other heavy items. These bags can be used for trips other than to the grocery store as well. Use CFL Light Bulbs Instead of Incandescent As your existing light bulbs die out, it’s time to switch them out for CFL light bulbs. These actually have two main benefits for you. The first is that they last up to 5 years longer than incandescent bulbs. Also, they utilize 70 percent less electricity when running. This is a major difference that can do wonders when it comes to your electric bill. Just imagine how much energy you could save when all the light bulbs in your home are running on 70 percent less power. Going eco-friendly isn’t really a hard thing to do. The difficult part is just understanding the small differences you can do each and every day that translates to the biggest impact. The above are three great ways to get started on your new eco-friendly lifestyle habits.
  21. Why Nature Conservation Is Important

    Nature differs for different animals, but it's suffering the same fate as well: The endangerment of many species and threats to the natural resources. The seascapes and landscapes, as well as the protection of the many wild species, are important to the economic, social and environmental well-being of our country's wildlife. Here are some reasons why nature conservation important Safeguards Human Life Almost 50 per cent of human medicines come indirectly or directly from the natural world. Many lifesaving drugs, such as anti-cancer drugs, originated in nature. 60% of people all over the world depend almost completely on plants for primary medication. Also, animals are used for traditional medicines in some parts of the world. Conserving and studying nature is as significant as other human health initiatives, and the conservation health benefits have to be included together with other discussions concerning saving nature. Conservation and wildlife science are relevant to our lives. Environmental Protection Having a healthy environment is vital to healthy living. The overall earth’s atmospheric temperature is increasing, that's why environment protection organisations and groups are making environmental protection steps to reduce ozone depletion. Marine Ecosystems Oceans are known to be the largest ecosystems and are also the largest life support systems on Earth. The oceans generate 50 per cent of the oxygen humans breath. Also, the ocean provides 16.6% of the animal proteins humans eat. The security, economy and survival of humans require a healthy ocean, that's why when you help to conserve it, this can bring many advantages to humankind. Natural Parks Health Natural parks are home to numerous endemic specie and they should be protected. These natural parks are important because they protect the areas of natural beauty, and it's a land that is set aside for animals, plants and where they live. Natural parks play a big role in keeping the environment healthy because they house many plants. The parks are also places for people to know more about native animals and plants and how they depend on each other. Habitat Conservation and Terrestrial Ecosystem Some species can't live outside the natural habitat without the intervention of humans, like the habitats found in an aquarium or zoo. Other migratory species tend to be vulnerable to habitat destruction since they inhibit two or more natural habitats. Like everything in life, nature doesn't operate in isolation; most of the species found on the reserve are usually migratory, hence their conservation does not rely solely on the reserve. For instance, many of the butterflies on the reserve also spend their time in urban environments such as in city parks or your backyard: Everything is connected. Natural habitat alteration can lead to a domino effect that will harm the whole ecosystem. Therefore, everyone has an important role to play in nature conservation. Small actions such as looking for landscape services, planting native species in the garden or recycling water bottles, to big actions such as investing in hundreds of thousands of trees, all help to keep our planet and nature healthy. For landscape services, click here.
  22. Plots of land where nothing has previously been developed on are quite rare these days, especially in urban areas. No matter if the land is purchased for farming or house building, checking the soil for contamination is extremely important, in order to avoid hazardous chemicals from coming in contact with anything that’s being developed on in or in the nearby sites. Up until recent years, environmental laws were more relaxed and it was not uncommon for waste was dumped close to where the products were used. Chemicals can persist in the soil for decades and can be really dangerous, especially if it comes in contact with crops or animals. Fortunately, there are multiple solutions that have been developed to treat the soil and restore its fertility. The Dangers of Soil Contamination To put it simply, soil contamination occurs when the soil comes in contact with pollutants, mostly due to hazardous past activities that were conducted on the site. The concentration of pollutants becomes higher than normal, often spreading to the nearby areas and polluting the neighbour lands as well. People have often reported dealing with contaminated soil, due to recent demolition or construction work developed close to their homes or farms. Living or working in close contact with contaminated soil increases the risk of chemical exposure through skin absorption or inhalation of chemicals. If corps are being planted on such lands, they can quickly absorb chemicals from the soils that travel from their roots to their leaves, fruits and seeds and eventually reach the people who consume the produce. Before coming in contact with the human body, soil contamination can also affect crop quality, by decreasing the fertility of the soil and alter its structure. The crops will develop poorly and, over time, the soil will become less productive and even completely infertile due to large quantities of toxic chemicals. Soil contamination can also lead to water pollution. After rain, the surface runoff can carry the polluted soil and mix it into different water sources. This way, the water fills with toxic chemicals, which make is unfit for humans, plants or animals. Low levels of contamination can produce reactions such as nausea, fatigue, rashes or headaches, while exposure to high levels of contamination can even result in neurological or reproductive disorders. Studies have reported that prolonged high chemical exposure can also increase the risk of cancer. The most vulnerable are usually elders, pregnant women and especially children, who often play in gardens and ingest soil particles from touching their mouth with dirty fingers. In such situations, the health risks are much higher. Common Soil Contamination Reasons In urban areas, lead is the most common soil contaminant, mostly because it used to be found in the compounds of exterior paint. It is very easy for old paint to disintegrate and fill the soil around the house with flakes that can contaminate it. Avoiding to grow crops or do digging near buildings that could have been painted with such old paint is one simple way to avoid contamination. Heavy metals and industrial chemicals are also present in urban areas, though they are more likely to be found in industrial areas, rather than residential. There is a wide range of activities that can lead to soil pollution, such as mining, that can release sulfuric acid, mercury and acid into the soil. Fuel storage can release hydrocarbons, while agricultural and industrial waste can pollute the soil due to leaks, spills or pipeline ruptures. Even light industrial or agricultural activities conducted on the site can result in some sort of contamination. Some of the most common reasons are: · Pesticides: after World War II, people started using DDT, an insecticide that turned out to be extremely dangerous for the environment, to deal with rodents, weeds and insects that threatened their crops. In 2011, traces of DDT were still found in human bodies, despite being banned almost 30 years ago. · Industrial pollution: improper disposal of chemical waste from various types of industries has led to soil acidification and contamination with heavy metals, oils and toxic chemicals. · Poor irrigation: bad irrigation practices have led to increased soil salinity, while improper maintenance of irrigation canals and intensive farming slowly degraded the soil over time. · Urban activities: disposal of solid waste is another form of soil pollution, most common from plastic or batteries, which contain lithium that causes soil leaching. Sewerage leaking can also damage soil quality or change its chemical composition. Dealing with Contaminated Soil Testing soil for contamination is quite easy and many laboratories offer such services. Private companies and public universities also offer soil testing services, which can reveal all the information needed. Some of these services are mail-in and the labs will provide instructions on how to properly collect soil samples and send them through. After the test reveals the level of pollution, there are a few procedures that can help deal with contaminated land. · Soil Washing: this is often considered to be the best technique to treat heavy metal and hydrocarbon contamination. Soil washing is a process that involves physically separating the contaminated particles from the soil by using heat or water to remove them. · Bio-piles: this process involves excavating the soil, forming it into piles and mixing it with soil amendments. The piles are enclosed and an irrigation system pumps air and nutrients through the soil. The treatment time varies between 3 and 6 months, after which the excavated soil is returned to its original location. · Soil Stabilization: typically used to treat sub-grade materials, such as clays or granular materials, the process is used to enhance the physical properties of the soil. It uses reduction and oxidation to incorporate additives into the soil, until it achieves the desired properties and the contaminated soil become non-hazardous. The decontamination process can vary, depending on the type of pollutants that are found in the soil and the contamination period. After decontamination, the disposal of the contaminated remains must be carried out according to local regulations, to avoid polluting other areas.
  23. Protein is mainly composed of chemical elements such as carbon, hydrogen, oxygen and nitrogen. It is an important biological macromolecule. All proteins are multimers formed by the connection of 20 different amino acids. After Forming proteins, these amino acids are also called as a residue. The boundaries between proteins and peptides are not very clear. Some people believe that the number of residues required for a functionally acting domain is called a polypeptide or peptide if the number of residues is less than 40. To function biologically, proteins need to be properly folded into a specific configuration, mainly through a large number of non-covalent interactions (such as hydrogen bonds, ionic bonds, van der Waals forces and hydrophobic interactions); in addition, in some proteins (especially in the case of secreted proteins), disulfide bonds also play a key role. In order to understand the mechanism of action of proteins at the molecular level, it is often necessary to determine the three-dimensional structure of a protein. Structural biology has been developed by studying protein structure, using techniques including X-ray crystallography, nuclear magnetic resonance, etc. to resolve protein structures. A certain number of residues are necessary to exert a certain biochemical function; 40-50 residues are usually the lower limit of the size of a functional domain. Protein size can range from such a lower limit up to thousands of residues. The current estimated average length of proteins differs between different species, typically about 200-380 residues, while eukaryotes have an average protein length of about 55% longer than prokaryotes. Larger protein aggregates can be formed by many protein subunits; for example, by the polymerization of thousands of actin molecules to form protein fibers. Discovery history In 1959, Perutz and Kendrew analyzed the structure of hemoglobin and myoglobin, solved the three-dimensional structure, and won the 1962 Nobel Prize in Chemistry. Pauling discovered the basic structure of the protein. Based on the X-ray diffraction data, Crick and Watson proposed a model of the three-dimensional structure of DNA. Received the 1962 Nobel Prize in Physiology or Medicine. After the 1950s, Hauptmann and Karle established a purely mathematical theory for the direct determination of crystal structures using X-ray analysis, which has epoch-making significance in crystal research, especially in the study of macromolecular biological substances such as hormones, antibiotics, and proteins. And the molecular structure of new drugs played an important role. They were awarded the 1985 Nobel Prize in Chemistry. Structure type Protein molecules are covalent polypeptide chains formed by the condensation of amino acids end-to-end, but natural protein molecules are not loose random polypeptide chains. Each natural protein has its own unique spatial structure or three-dimensional structure, which is often referred to as the conformation of the protein, ie the structure of the protein. The molecular structure of a protein can be divided into four levels to describe its different aspects: Primary structure: A linear amino acid sequence that makes up a protein polypeptide chain. Secondary structure: a stable structure formed by hydrogen bonds between C=O and N-H groups between different amino acids, mainly α-helix and β-sheet. Tertiary structure: The three-dimensional structure of a protein molecule formed by the arrangement of multiple secondary structural elements in three dimensions. Quaternary structure: used to describe a protein complex molecule that is functionally formed by interactions between different polypeptide chains (subunits). In addition to these structural levels, proteins can be transformed in multiple similar structures to perform their biological functions. For functional structural changes, these tertiary or quaternary structures are usually described in a chemical conformation, and the corresponding structural transformation is referred to as a conformational change. About us Our products and services are used worldwide in research fields for diverse applications, including basic research, drug discovery, and diagnostic study. Here are some our products like: Cryo-EM,membrane proteins,virus-like particle service,VLP construction,etc.
  24. Adjuvant Selection is the main method for finding molecular genetic markers, vaccines like bacterial vaccines, cancer vaccines, RNA vaccines, MAS breeding and so on. Major methods for finding molecular genetic markers DNA markers are divided into two types: type Ⅰ markers, mainly are some single genes, and used to compare the homologous loci varieties of relative distance and chain and linear correlation; Ⅱ type markers, mainly high polymorphism, information content rich DNA fragments, is one of the most commonly used microsatellite marker. Through Adjuvant Optimization, more and more kinds of molecular markers were introduced, including restricted fragment length polymorphism (RFLP), random amplified polymorphic DNA (RAPD), amplified fragment length polymorphism (AFLP), and Microsatellites. At present, there are 2,505 markers in the world's pig research, including 1,391 microsatellite markers. Ⅰ type 873, type Ⅱ mark 1632. The main methods to search for molecular genetic markers are candidate gene method and genome scanning method. 1. Candidate gene method as a candidate gene for a trait, it is usually some genes whose biological functions and nucleic acid sequences are known, and they are involved in the growth and development process of the trait. These genes may be structural genes, regulatory genes or genes that affect the expression of traits in biochemical metabolic pathways. Candidate gene method research should follow certain steps, such as candidate gene selection primer design, gene specific fragment amplification, polymorphic locus search and so on. Candidate gene search USES genes that are thought to have a direct physiological function for a trait to find QTLS. In addition, genes found in other species that control some traits can be studied as candidate genes for pigs. For example, the h-fabp gene affects the backfat thickness and intramuscular fat content of pigs (Gerbens et al., 1999). 2000; 2001); The melanocorticoid receptor 4 (MC4R) gene was significantly correlated with the intake, backfat thickness and growth rate of pigs (Kim et al., 1999; 2000). 2. Genome scanning: all genetic information is stored on the 19 pairs of chromosomes of the pig. Reference families were established, such as meishan European and American pig species, wild boar big white pig, and their hybrid offspring were used to find QTL through genetic markers. The most effective design is the genotype analysis of F2 generation isolation population. Figure 4-2 is a simple schematic diagram of single genetic marker and linkage QTL analysis. Alleles of genetic markers and their linkage QTL in F1 generation were heterozygous. In the F2 generation isolation population, the ratio of the three possible genotypes per seat should be 1:2:1, when the average performance of marker genotypes is compared, the existence of linkage QTL can be analyzed. Anderson (1994), such as reported with a wild boar by the results of the large white building reference group, using the 105 DNA markers in the genetic map, the separation of F2 generation 200 pigs linkage analysis research found that on chromosome 4 seat back fat and control the growth rate, the average genetic effect 24 g/d and 5 mm, respectively, the equivalent of F2 DaiQun total phenotypic variation of 12% and 18%. Daily weight gain can differ by more than 50g between two extreme homozygous genotypes, resulting in a 10kg weight difference at market time in pigs. (iii) MAS breeding In pig breeding selection, it is difficult to determine the sex efficiency of low heritability (e.g., reproductive traits), high cost of measurement (e.g., disease resistance), phenotypic values (e.g., lean meat rate) or limited sexual performance (e.g., milk production) early in development. It is estimated that the selection of the marker before the determination of the offspring can increase the selectivity response by 10%~15%. The MAS of compatriots who choose to combine can be increased by about 40%. Combining multiple genetic markers and trait information, the selectivity response can be increased by 50%~200%. Using marker selection in cross breeding can predict and make full use of heterosis. Molecular genetic markers can also be applied to early selection and screening and detection of large populations to select populations with desired genotypes. For example, there is little progress in the improvement of pig litter, a low genetic trait, by traditional methods. Rothschild et al. found in 1994 that the estrogen receptor (ESR) gene was one of the main genes responsible for the litter size of pigs, which could control the total litter size of 1.5 pigs and the live litter size of 1 pig in the meishan synthetic line of China. In the Chinese two-flower face hybrid population, the agricultural university of China not only confirmed the results of Rothschild et al., but also found another main gene locus controlling the number of piglets - FSH, which can control the total number of piglets and the number of live piglets by 2.0. Although MAS can improve the effectiveness of selection and the annual amount of genetic improvement, its effectiveness is also affected by many factors. In addition to the heritability of traits, the intensity of selection, and the size of the selected population, the determinants are the linkage between genetic markers and QTLS. Zhang (1992) pointed out that each QTL could be specifically detected by using genetic markers closely linked to QTL, and the final selection of genetic markers would be equivalent to the selection of QTL itself. Therefore, genetic markers closely related to QTL must be obtained in order to improve MAS efficiency. Resources at present, through the establishment of the pig family, has some related to the growth, reproduction and carcass, meat quality of QTL mapping in some microsatellite nearby, such as on chromosome 3 microsatellite Sw2427 - Sw251 area and daily gain of pigs, on chromosome 4 S0101 - S0107 area and back fat belly fat, 7 chromosome S0064 S0066 regional composition and has a strong correlation between birth weight and body. It can be predicted that with the discovery of more genetic markers closely linked to QTL, MAS will be applied more effectively in practical breeding.
  25. 3 Cancer vaccine adjuvant selection The initial aim of formulating vaccines in adjuvants was to deliver the antigen in a poorly metabolizing and slowly degrading substance. The intention was to favor the slow and sustained release of the antigen to be captured by antigen-presenting cells (APCs) and be subsequently presented to T cells. Aluminum salts are widely used to favor T helper cell 2 (Th2)-mediated humoral immunity, but they are less efficient for promoting Th1-dependent immunity. To this aim, water-in-oil adjuvants have been developed to create a depot of the antigen at the site of the injection. The next generation of vaccine delivery agents includes nanoparticles such as silica or liposomes or synthetic polymers, which are ideal vehicles to be taken up by dendritic cells (DCs) patrolling within the subcutaneous tissues. However, the challenge with such supports is to selectively promote DC uptake while eluding the systemic reticuloendothelial network of macrophages, which routinely clear circulating particles. In addition to these substances designed to favor delivery of the antigen to APCs, today’s therapeutic vaccines also contain another class of adjuvants aimed to deliver danger signals to activate the immune system, as antigen alone may fail to prime effective T cell responses or even induce tolerance. 4 The choice of cancer vaccine delivery system The choice of delivery systems and route of immunization depends on the end use of the vaccine. For practical reasons and minimal side effects, most prophylactic vaccines are administered via the skin, usually by subcutaneous injections in the epidermis or the dermis. These two locations are ideal, as they are enriched respectively in Langerhans DCs and dermal DCs, both cell populations being very efficient in capturing and processing antigens. The oral route is also very convenient and is used by vaccines against polio, typhoid fever, cholera, and rotavirus. The oral route is, however, more challenging in view of the extreme conditions in the gastrointestinal tract, including the low pH in the stomach and the presence of microbiota, which may degrade the antigen before it reaches the lymphoid organs. Moreover, the usually tolerogenic gut environment may not be ideal to generate a strong systemic immune response. With regard to therapeutic vaccines used to treat chronic noncontagious diseases such as cancer, atopy, or diabetes, both immediate cellular effector responses and long-term immunity are desired to guarantee the continuous immune-surveillance of the disease. Although prophylactic vaccines for global immunization programs must be simple, inexpensive, and given via a noninvasive route, therapeutic cancer vaccines can benefit from more complicated technologies and use more invasive routes of delivery if beneficial for the patient. There is a very large array of cancer vaccines under development which use various delivery systems, and which are being tested in clinical trials. Other delivery routes tested in therapeutic cancer vaccines range from subcutaneous and intradermal to more invasive intraperitoneal and intranodal injections, to optimize antigen uptake by APCs and favor a local potent immune response. For instance, particulate therapeutic vaccines such as virosomes or nanoparticles can be injected in LNs using an ultrasound-guided imaging procedure. Although most of these strategies are still in the development stage, the potential to achieve strong and long-lasting antitumor responses is high, owing to new delivery systems and better understanding of T cell memory development. Reference [1] FUTURE II Study Group. Quadrivalent vaccine against HumanPapillomavirns to prevent high-grade cervical lessions. N Engl J Med, 2007, 356(19): 1915 [2] Olsson SE, Villa LL, Costa RLR, et a1. Induction of inmmne memory following administration of a prophylactic quadrivalent human papillomavirus (HPV) types 6/1 1/16/18 LI virus-like particle (VLP) vaccine. Vaccine, 2007 (25): 4931 [3] Harris JE, Ryan L, Hoover Jr HC, et a1. Adjuvant active specific immunotherapy for stage II and III colon cancer with an autologous tumor cell vaccine: Eastern Cooperative Oncology Group Study E5283. J Clin Orwol, 2000, 18(1): 148 [4] Berd D, Maguire Jr HC, Mastrangelo MJ, et a1. Treatment of human melanoma with a hapten — modified antologous vaccine. Ann NY Acad Sci, 1993, 690(8): 7 [5] Remann R, Goldschmidt AJ, Richter A. Adjuvant therapy of renal cell carcinoma patients with an autologous tumor cell lysate vaccine: a-year—follow—up analysis AnticancerRes, 2003, 23(2A): 969 [6] Mitchell MS, Kan — Mitchell J, Kempf RA, et a1. Active specific im-munotherapy for melanoma: phase I trial of allogeneic lysates and a novel adjuvant. Cancer Res, 1988, 48(20): 5883
  26. 3 Benign Mucous Membrane Pemphigoid 3.1 Clinical manifestations Conjunctival and oral mucosal damage accounted for 60% to 90%, patients with nasal, pharyngeal, genital and anal mucosa accounted for about 25%, skin involvement is rare, skin damage is very similar to the lesions of bullous pemphigoid, but the time is short, and the stenosis or adhesion caused by scar healing and scar formation is characteristic. 3.1.1 Eye damage The eye is the only affected part, and the damage usually occurs asymmetrically. After 1 to 2 years, the contralateral eye mucosa is involved. There are symptoms of catarrhal conjunctivitis. Transparent blisters can be found and quickly ruptured. Subsequently, scar atrophy, conjunctival and bulbar conjunctiva adhesions, eye movement involvement, tendon varus leading to secondary corneal changes, corneal opacity, scar formation of the tarsal plate with mucosa, atrophy of the gland and blockage of the lacrimal duct, thus corneal dryness, discoloration and blinding ulcers are formed. 3.1.2 Mucosal damage Multiple blisters quickly form painful erosions and the scars heal. If the damage occurs in the tongue ligament, the contracted scar can limit the movement of the tongue. Damage that occurs in soft palate, tonsil, and buccal mucosa may limit food intake. The genital area of the vulva can form a head adhesion, a vaginal stenosis, and the like. 3.1.3 Skin damage The incidence of skin damage is only about 25%, the damage is a tension blisters, the blister wall is not easy to rupture, occurs on erythematous skin, one or more parts. Healed with atrophic scars. If bullae occur in the head, scarring hair loss may occur. Generalized lesions are extremely rare, and even if there are secondary scar formation. Benign mucosal pemphigoid can occur repeatedly for several years without significant effect on general health. The faster the disease progresses, the worse the prognosis. Due to eating difficulties, malnutrition and cachexia may occur, and the incidence of blindness is approximately 20% to 60%. Although extremely rare, there have been reports of cancerous changes in the scars of the oral mucosa. 3.2 Laboratory examination 3.2.1Histopathology: typical epidermis blister, no spine release. Infiltration of inflammatory cells composed of lymphocytes, plasma cells, and eosinophils can be seen in the upper dermis. Subsequently, there were a large number of fibroblasts with superficial dermal fibrosis and vascular hyperplasia and scar contracture. 3.2.2 Immunofluorescence: direct immunofluorescence of skin mucosa to detect IgG and C3 deposition in the basement membrane zone, and IgA and C3 deposition were also observed. The homogenous linear deposition was almost the same as that in bullous pemphigoid. The positive rate of indirect immunofluorescence detection of anti-basal membrane circulating antibodies was <10%, and the titer was low. If the DIF is negative, the fresh tissue should be removed from the erythema around the lesion for repeated testing. 4 Pathogenesis of Pemphigus In the plasma of patients with pemphigus, there is anti-Dsg3 and/or anti-Dsg1 IgG, and no anti-Dsg2 antibody exists. This autoreactive antibody binds to its corresponding antigen, leading to a series of clinical pemphigus. The emergence of performance. In the active phase of pemphigus vulgaris, the serum is mainly pathogenic IgG4 subclass and IgG1, while in the serum of patients with long-term remission, there are low-valency IgG1 subclasses, IgG4 and Dsg1 and Dsg13 on keratinocytes. The combination causes the loss of adhesion between cells, leading to the release of intercellular cells and the formation of blisters in the epidermis. The antigen Dsg produced in the MMP autoimmune disease belongs to the transmembrane component of desmos, belonging to the cadherin superfamily in the adhesion molecule, whose gene is located at 18q12.1. Dsg is divided into three categories: Dsg1, Dsg2, and Dsg3. Among them, Dsg2 is expressed in all tissues with desmosome, including monolayer epithelial cells and myocardial tissue. Dsg1 and Dsg3 are mainly restricted to stratified squamous cells. Current studies have shown that Dsg1 and Dsg3 are target antigens of pemphigus foliaceus (PF) and pemphigus vulgaris (PV), respectively. The relative molecular mass of Dsg3 is about 130 kD. which is mainly distributed on the surface of keratinocytes in the basal layer of the epidermis and the upper layer of the basal layer. The relative molecular mass of Dsg1 is about 160 kD, which is mainly distributed on the keratinocyte membrane in the upper layer of the epidermis, with the advantage of granular layer and subgranular layer expression. The Dsg3 and Dsg1 molecules, like other cadherin molecules, have five tandem repeats of approximately equal size extracellular domain (EC), each of which is approximately 100 amino acid residues in length, of which EC1 the region corresponds to the extracellular amino terminal residue and EC5 is at the carboxy terminus. The difference between Dsg1 and Dsg3 is mainly due to the homology of the 1 to 4 extracellular domains of Dsg1 and the homology of the 5 extracellular domains of Dsg3. Unlike classical cadherins, Dsg1 has a longer intracellular fragment, and the extracellular fragment of Dsg3 is slightly longer than Dsg1, but its intracellular domain is slightly shorter and has no glycine/serine-rich region. In the five extracellular domains of the pemphigus antigen, EC1, EC2, and EC4 have relatively large homology and can be specifically recognized by the plasma of pemphigus patients. Therefore, these epitopes are called "an immune-dominant epitope, or a "pathogenic epitope," an antibody that specifically recognizes an epitope is called a "pathogenic antibody." The pemphigus antigen contains at least one "pathogenic epitope" in the EC1 -2 region, and antibodies against EC1 -2 are closely related to the pathogenesis of pemphigus. The recombinant protein expressed by the EC1 -2 and EC3 -4 gene sequences of Dsg3 only reacted with the plasma of pemphigus patients, and the response rates of the two were 57.9 % and 52.6%, respectively, and the bullous pemphigoid, system Lupus erythematosus and normal people do not respond. This indicates that EC1 -2 and EC3 -4 are antigen-specific and have a high affinity with pemphigus antibodies, thus providing a new approach for serological diagnosis and identification of pemphigus. In Dsg1 and Dsg3, when either function is lost, the other can partially compensate for its function. This theory explains the tissue specificity of the loss of intercellular adhesion caused by autoantibodies in pemphigus patients. Because Dsg1 and Dsg3 have a certain distribution pattern, the difference in anti-Dsg antibodies also leads to differences in the clinical manifestations of pemphigus. By inserting the Dsg1 gene into Dsg3 knockout mice to form a transgenic mouse capable of expressing Dsg1, it was found that Dsg1 can compensate for partial Dsg3-mediated loss of intercellular adhesion function, which is confirmed genetically. 5 Treatment Glucocorticoid is preferred for the treatment of pemphigus. Most scholars at home and abroad are empirical drugs. There are ethnic and regional differences in the choice of hormone dose. At present, the severity of the disease is not unified by using the scoring system. If the two are linked to the hormone dose and applied to the clinic, the treatment plan will be more reasonable. Determine the initial dose of hormone according to the ABSIS system: ABSIS skin severity score ≤10, give 30 ~ 40 mg / d, skin score of 10 ~ 50, 60 mg / d is appropriate, skin score > 50 points, give 80 mg /d. If the skin lesions are not controlled for 5 to 7 days, increase the dose by 50%. Reduced indications: Daily new blistering number <5, no new erythema; no obvious exudation of erosion surface; pemphigus antibody titer decreased earlier; ABSIS skin score decreased by more than 35%. The long-term use of large doses of hormones can easily lead to many drug reactions. Therefore, the combination of immunosuppressive agents, including azathioprine, cyclophosphamide, mycophenolate mofetil, etc., is generally used to reduce the number of hormones and shorten the treatment time. At the same time, it can be combined with an immune-modulator (Amlalazine, etc.), plasma exchange method and in vitro. Photochemotherapy, etc. Randomized controlled observation of prednisone combined with mycophenolate mofetil, azathioprine and prednisone alone in the treatment of 42 cases of pemphigus, combined with the ABSIS system to assess the severity of the disease before and after treatment, the results show that the three treatment days The short-term efficacy and safety of acne are similar, but prednisone combined with mycophenolate mofetil reduces the dose of hormones most significantly. In recent years, some biological agents and treatments have become new choices for the treatment of pemphigus, such as rituximab, high-dose intravenous immunoglobulin (IVIG), immunosorbent assay, TNF-α antagonist and hematopoietic stem cell transplantation therapy. For the severe bullous disease such as pemphigus, detecting the Dsg ELISA index has certain guiding significance for judging its severity. However, if medical workers are to accurately grasp the changes in their condition, they also rely on an effective and widely recognized scoring system to provide a reliable clinical basis for the treatment and adjustment of pemphigus. At present, there are few clinical applications of ABSIS and PDAI. Both have their own advantages and disadvantages. If they can be combined, it is expected to improve the evaluation method. The correlation between the disease scoring system and antibody levels, and the number of hormones controlled by scoring will be important research topics. Many new drugs and treatments have emerged in recent years, and multi-center large-scale clinical trials are still needed to explore the best treatment options. Reference [1] Barnadas MA, Rubiales MV, Gich I, et al. Usefulness of specific anti-desmoglein 1 and 3 enzyme-linked immunoassay and indirect immunofluorescence in the evaluation of pemphigus activity [J]. Int J Dermatol, 2015, 54(11): 1261-1268. [2] Daneshpazhooh M, Kamyab K, Kalantari MS, et al. Comparison of desmoglein 1 and 3 enzyme - linked immunosorbent assay and direct immunofluorescence for evaluation of immunological remission in pemphigus vulgaris [J]. Clinical & Experimental Dermatology, 2014, 39(1): 41-47. [3] Nakahara T, Takagi A, Yamagami J, et al. High anti-desmoglein 3 antibody ELISA index and negative indirect immunofluorescence result in a patient with pemphigus vulgaris in remission: evaluation of the antibody profile by newly developed methods [J]. Jama Dermatology, 2014, 150(12): 1327-1330. [4] Pfutze M, Niedermeier A, Eming R. Introducing a novel autoimmune bullous skin disorder intensity score ( ABSIS) in pemphigus [J]. Eur J Dermatol, 2007, 17(1): 4-11. [5] Murrell DF, Dick S, Amagai M, et al. Consensus statement on definitions of disease, end points, and therapeutic response for pemphigus [J]. J Am Acad Dermatol, 2008, 58(6): 1043-1046. [7] Chams-Davatchi C, Rahbar Z, Daneshpazhooh M, et al. Pemphigus vulgaris activity score and assessment of convergent validity [J]. Acta Med Iran, 2013, 51(51): 224-230. [8] Sebaratnam DF, Frew JW, Davatchi F, et al. Quality -of-Life Measurement in Blistering Diseases [J]. Dermatol Clin, 2012, 30(2): 301-307. [9] Mahajan VK, Sharma NL, Sharma RC, et al. Twelve-year clinicotherapeutic experience in pemphigus: a retrospective study of 54 cases [J]. Int J Dermatol, 2005, 44(10): 821-827. [10] Agarwal M, Walia R, Kochhar AM, et al. Pemphigus Area and Activity Score (PAAS) --a novel clinical scoring method for monitoring of pemphigus vulgaris patients [J]. Int J Dermatol, 1998, 37(2): 158-160.
  27. Life is hectic and people want their homes and gardens to be attractive and low maintenance. It is why composite deck boards are so suitable for outdoor living – they don’t need to be stained and they don’t splinter or rot. True, composites do fade just a little bit at first from sun exposure, but then they settle down and the fading stops. Trendy for Residential- or Commercial Properties Composite boards are sought after for the residential market as well as for business properties. Composite decking suppliers have hollow- or solid boards which can be used for garden decking – patios, swimming pool decks, sun decks, entertainment areas and more. Making use of a wood plastic composite material, the plastic decking makes sure you can enjoy the beauty of the outdoors without worrying about ongoing maintenance. You get lots of options too – decks in lots of colours and textures. Less Seams and Screws than Wood Also, wood planks are essentially sold as 2.9mboards, but composite deck boards are much longer. The advantage of this is that you have fewer seams on the deck. With composite decking, you can use stainless steel decking screws, while products also come with a clip or tongue-and-groove assembly. You don’t see unsightly rows of screw heads. Installing composite decks is quick too with joining systems. Coping with all kinds of Weather Whatever trendy aesthetic features you’re looking for with composite deck, there are different shades to choose from. With composite boards, you can get truly creative. These boards have also been designed to cope with different climates without you having to worry about staining too soon. Known also as Wood-Plastic Composite, this man-made material even has the natural look and feel of a hardwood floor. Many composites are made from recycled plastic and wood flour mixture, making them far friendlier on the environment than other deck types. Most boards are made from Polyethylene or Polyvinyl Chloride and you can buy them from a store or online. The Look of Real Wood A beautiful deck simply becomes an outdoor extension of a home, and it cleverly mimics the look of real wood. It will look amazing and the best part there’s no painting, oiling or staining needed. You simply wipe it down with warm water and a gentle cleaning product. r, so you can be sure your deck will look brand new year after year. The best part about these boards is that you can say good-bye to old greying, warped, splintered wood which clashes with your sparkling pool. Rather welcome a stylish composite deck that looks beautiful in all kinds of weather year in and year out.
  28. What is 3D cell culture? Three-dimensional cell culture is based on the common three-dimensional culture model of the scaffold, which can better simulate the natural environment in which the cells grow. Three-dimensional cell culture (TDCC) refers to the co-culture of vectors with different materials in three dimensions and various kinds of cells in vitro, so that cells can migrate and grow in the three-dimensional spatial structure of the carrier. Three-dimensional cell-carrier complex. Frontier knowledge about 3D cell culture research Three-dimensional cell tissue plus tensile culture model of the United States flexcell company Tissue Train tensile stress stimulation three-dimensional hydrogel stent cell tissue culture system. Functional highlights of the three-dimensional cell tissue augmentation culture model: after burning three-dimensional cell tissue culture and stretching three-dimensional cell tissue culture in the true sense of three-dimensional culture - the system with a variety of coated surfaces (Amino, Collagen (Type I Or IV), Elastin, ProNectin (RGD), Laminin (YIGSR) collagen hydrogels for extracellular matrix scaffolds in biomaterial scaffold studies, compared to traditional nanofiber scaffolds and porous scaffolds, hydrogel scaffolds The network contains a lot of water, which can supply cell nutrients well, and can also cross-link bioactive factors to regulate cell growth and differentiation. Therefore, hydrogel scaffolds can better simulate the tissue-like physics required for cell growth. The spatial structure has high plasticity, relatively simple manufacturing process and convenient clinical application. Three-dimensional cell tissue pressure-carrying culture system model of American three-dimensional cell tissue after-force culture model Three-dimensional cell culture in three-dimensional cell culture 1) The system provides periodic or static pressure loading of various tissue, three-dimensional cell cultures; 2) based on the deformation of the flexible film substrate, uniform force; 3) Real-time observation of the reaction of cells and tissues under pressure; 4) can selectively block stress loading on cells; 5) Simultaneously have multi-channel cell pull force loading function; 6) Up to 4 channels, 4 different programs can be run simultaneously, and multiple different pressure deformation rate comparison experiments are performed; 7) Multiple frequencies (0.01-5 Hz), multiple amplitudes and multiple waveforms can be operated in the same program; 8) Better control of waveforms under ultra-low or ultra-high stress; 9) A variety of waveform types: static waveform, positive rotation waveform, cardiac waveform, triangular waveform, rectangle and various special waveforms; 10) computer system for pressure loading cycle, size, frequency, duration precise intelligent control typical application range: detection Biochemical reactions of various tissues and cells under pressure. Three-dimensional cell tissue augmentation culture model. Three-dimensional cell tissue stretchestensile force loading culture system model of American flexcell company Three-dimensional cell culture three-dimensional cell tension loading culture 1) The system provides axial and circumferential stress loading on two-dimensional, three-dimensional cells and tissues; 2) based on the deformation of the flexible film substrate, uniform force; 3) The reaction of cells and tissues under stress can be observed in real time; 4) can selectively block stress loading on cells; 5) Simultaneous multi-channel cell pressure loading function; 6) In combination with the Flex Flow parallel slab flow chamber, fluid shear stress can be applied while pulling the cells; 7) Up to 4 channels, 4 different programs can be run simultaneously, and multiple different tensile deformation rate comparison experiments are performed; 8) Multiple frequencies, multiple amplitudes and multiple waveforms can be operated in the same program; 9) Better control of waveforms under ultra-low or ultra-high stress; 10) Multiple waveform types: static waveform, positive rotation waveform, cardiac waveform, triangular waveform, rectangle, and various special waveforms; 3 Three-dimensional cell cultures in life applications: Customized 3D cell culture services are common in our lives, and there are also 3D cell culture related products on the market. Creative Bioarrayoffers 35 human cell systems with over 160 different cell types. Moreover, we also provide our customers primary cells from over 13 types of other animals. These cells taken from living tissue are extremely accurate as they are literally coming from the source and are available from many sources on the human body. These living samples can give extremely accurate information about the cells in vivo and give relevant information regarding the living systems. Not only canCreative Bioarray offer such a wide range of primary cells of humans, but we also have a selection of primary cells of animals for comparative testing. Bone cells, which are found within the bone tissue, are responsible for bone production, maintenance and modeling. There are three different types of cells that found only in the bone. The osteoblasts are derived from mesenchymal stem cells and its function is bone matrix synthesis and its subsequent mineralization. The osteoclasts are large cells that dissolve the bone and osteocytes are cells inside the bone. At Creative Bioarray, we offer 6 types of human primary bone cells including: Human Bone marrow-derived endothelial Cells, Human Osteoblast Cells, Human Osteoblasts (HOB), Human Osteoblast Cells (Postnatal), Human Calvarial Osteoblasts (HCO) and Human Osteoblasts-femural (HO-f). The method we use to isolate endothelial cells was developed based on a combination of established and our proprietary methods. These cells are pre-coated with PECAM-1 antibody, following the application of magnetic beads pre-coated with secondary antibody. Human osteoblasts may be used for various types of in vitro, in vivo, or regenerative medicine studies in normal or diseased systems. In addition, they may be used in bone development studies.
  1. Load more activity