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Enzyme immunoassay for the quantitative determination of anti-S1 IgA in human serum and plasma
The Matriks Biotek CORONAHUNTER® Q-CORS1 IgA ELISA has been especially developed for the quantitative analysis of anti-S1 IgA in serum and plasma samples. CORONAHUNTER® “real” quantitative ELISA kits for Sars-Cov-2 are now available to measure the “absolute” values of IgA!
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-S1 IgA in human serum and plasma
The Matriks Biotek CORONAHUNTER® Q-CORS1 IgA ELISA has been especially developed for the quantitative analysis of anti-S1 IgA in serum and plasma samples. CORONAHUNTER® “real” quantitative ELISA kits for Sars-Cov-2 are now available to measure the “absolute” values of IgA!
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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文献和实验小鼠抗IgA抗体(anti-IgA-Ab)酶联免疫分析(ELISA)
小鼠 抗IgA 抗体 (anti-IgA-Ab) 酶联免疫 分析( ELISA ) 试剂 盒使用说明书 本试剂仅供研究使用 目的:本试剂盒用于测定小鼠血清,血浆及相关液体样本中 抗IgA抗体(anti-IgA-Ab) 的 含量。 实验原理 : 本试剂盒应用双 抗原 夹心法测定 标本 中 小鼠 抗IgA 抗体 (anti-IgA-Ab) 水平。用纯化的 抗原 包被微孔板,制成固相 抗原 ,往包被单抗的微孔中依次加入 抗IgA 抗体 (anti
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
Diagnosis of Q Fever Using Indirect Microimmunofluorescence
on these slides, then rinsed and overlaid with anti-IgG, -IgM and/or IgA secondary antibodies. Finally, the slides are examined under a fluorescence microscope for presence of C. burnetii .
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