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。
载脂蛋白C2(apo-C2)是一种蛋白质，由APOC2基因编码。它在血浆中分泌，是极低密度脂蛋白和乳糜微粒的组成部分。它可激活毛细血管中的脂蛋白脂肪酶，水解甘油三酯，从而为细胞提供自由脂肪酸。该基因的突变导致高脂蛋白血症IB型，特点是黄瘤、胰腺炎和肝脾肿大，但没有增加动脉硬化的风险。实验室检查会显示血液中甘油三酯、胆固醇和乳糜微粒的水平升高。 本试剂盒采用双抗体夹心法酶联免疫吸附试验（ELISA）。往预先包被有人载脂蛋白C2(Apo-C2)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载脂蛋白C2(Apo-C2)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 Apo-C2. 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 Apo-C2 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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