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- MATRiKs Biotek
- 土耳其
- COR-QNS-IGM-STRIM
- 2025年08月29日
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Enzyme immunoassay for the quantitative determination of anti-spike Trimer IgM in human serum and plasma
The Matriks Biotek CORONAHUNTER® Q-CORS IGM ELISA has been especially developed for the quantitative analysis of anti-spike Trimer IgM in serum and plasma samples. CORONAHUNTER® “real” quantitative ELISA kits for Sars-Cov-2 are now available to measure the “absolute” values of IgG-A-M-E!
Various NIBSC* sera and panel sera, with the catalog numbers; NIBSC 20/B764, NIBSC 20/130, NIBSC 20/162, NIBSC 20/B770 determined with CORONAHUNTER® ELISA kits listed above.
*The National Institute for Biological Standards and Control (NIBSC) is the world’s major producer and distributor of WHO International standards and reference materials.
Enzyme immunoassay for the quantitative determination of anti-spike Trimer IgM in human serum and plasma
The Matriks Biotek CORONAHUNTER® Q-CORS IGM ELISA has been especially developed for the quantitative analysis of anti-spike Trimer IgM in serum and plasma samples. CORONAHUNTER® “real” quantitative ELISA kits for Sars-Cov-2 are now available to measure the “absolute” values of IgG-A-M-E!
Various NIBSC* sera and panel sera, with the catalog numbers; NIBSC 20/B764, NIBSC 20/130, NIBSC 20/162, NIBSC 20/B770 determined with CORONAHUNTER® ELISA kits listed above.
*The National Institute for Biological Standards and Control (NIBSC) is the world’s major producer and distributor of WHO International standards and reference materials.
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文献和实验Anti-PEG IgM Production via a PEGylated Nano-Carrier System for Nucleic Acid Delivery
of the ABC phenomenon. This chapter introduces a method for the evaluation of serum anti-PEG IgM by a simple ELISA procedure, and describes some precautions associated with this method.
CANDOR BIOSCIENCE: 关于ELISA板稳定性的技术探讨与比较
化合物溶液相比，具有更多的优势，而不仅仅是进一步提高了板的稳定性。 Figure 1: Calibration curves of an ELISA that was either blocked only with BSA (left panel) or blocked with BSA and additionally stabilized with Liquid Plate Sealer® (right panel). Calibration curves at the starting day
测定，可以采用竞争法模式。其原理是标本中的抗原和一定量的酶标抗原竞争与固相抗体结合。标本中抗原量含量愈多，结合在固相上的酶标抗原愈少，最后的显色也愈浅。小分子激素、药物等ELISA测定多用此法。2.2.6 捕获包被法测抗体（经典方法）IgM抗体的检测用于传染病的早期诊断中。间接法ELISA一般仅适用于检测总抗体或IgG抗体。如用抗原包被的间接法直接测定IgM抗体，因标本中一般同时存在较高浓度的IgG抗体，后者将竞争结合固相抗原而使一部份IgM抗体不能结合到固相上。因此如用抗人IgM作为二抗，间接测定IgM
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