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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解整合素金属蛋白酶10也被称为ADAM10或CDw156或CD156c，是一种由ADAM10基因编码的蛋白。该基因编码一个ADAM家族成员，可裂解许多蛋白质，包括TNF-α和E-cadherin。ADAM10是一种脱落酶，对肽类水解反应有广泛的特异性。它在两个细胞表面之间形成的Ephrin/eph复合物内，裂解Ephrin。在神经元中，ADAM10是最重要的酶，具有α-分泌酶活性，可对淀粉样前体蛋白进行蛋白加工。 本试剂盒采用双抗体夹心法酶联免疫吸附试验（ELISA）。往预先包被有人解整合素金属蛋白酶10(ADAM10)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解整合素金属蛋白酶10(ADAM10)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 ADAM10. 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 ADAM10 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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