BioReagent 级 ，适用于对基线干扰要求严格的色谱和分析工作流程。
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在色谱分析、有机合成和交叉偶联反应领域已被 0 篇同行评审文献引用。
补体受体1型（CR1）也被称为C3b/C4b受体或CD35（分化群35），是一种由CR1基因编码的蛋白质。它是补体激活调节因子（RCA）家族的成员。它介导细胞与激活补体的颗粒和免疫复合物的结合。它是处理和清除补体的免疫复合物的主要系统。已有研究表明，它可作为补体级联的负调节器，介导免疫粘附和吞噬作用。CR1分子的数量随着红细胞的老化而减少，在病理情况下，如系统性红斑狼疮（SLE）、HIV感染、一些溶血性贫血和其他以免疫复合物为特征的情况下，CR1分子也会减少。 本试剂盒采用双抗体夹心法酶联免疫吸附试验（ELISA）。往预先包被有人可溶性补体受体1(sCR1)捕获抗体的微孔中，依次加入样本、标准品、生物素标记的检测抗体，HRP酶结合物，中间经过温育和洗涤，用底物TMB显色，TMB在过氧化物酶(HRP)的催化下转化成蓝色，并在酸的作用下转化成最终的黄色。颜色的深浅和样本中的人可溶性补体受体1(sCR1)呈正相关。用酶标仪在450nm 波长下测定吸光度（OD值），计算样本浓度。
This kit employs the sandwich enzyme-linked immunosorbent assay (ELISA) principle. Microplate wells are pre-coated with a capture antibody specific to Human sCR1. Following this, the sample, standards, a biotin-conjugated detection antibody, and an HRP (horseradish peroxidase)-labeled conjugate are added sequentially to the wells. The procedure involves incubation and wash steps between each addition. For detection, TMB substrate is used. TMB yields a blue color in the presence of the peroxidase activity of HRP. The reaction is then stopped with an acid solution, which converts the blue color to a final yellow color. The intensity of the yellow color is directly proportional to the concentration of Human sCR1 present in the sample. The optical density (OD) is measured at a wavelength of 450 nm using a microplate reader. Finally, the concentration of the target analyte in the sample is calculated based on the standard curve generated from the standards.
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