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C-III也被称为apo-CIII，和载脂蛋白C3，由APOC3基因编码的蛋白质。它由肝脏和小肠分泌，存在于富含甘油三酯的脂蛋白上，如乳糜微粒、极低密度脂蛋白（VLDL）和残余胆固醇。载脂蛋白-III是一个相对较小的蛋白质，含有79个氨基酸，可以在苏氨酸-74处糖基化。最丰富的糖型的特点是O型二糖半乳糖与N-乙酰半乳糖胺（Gal- GalNAc）相连，进一步用最多两个唾液酸残基修饰。含量较少的糖型的特点是具有更复杂和岩藻糖基化的糖基。 本试剂盒采用双抗体夹心法酶联免疫吸附试验（ELISA）。往预先包被有小鼠载脂蛋白C3(Apo-C3)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小鼠载脂蛋白C3(Apo-C3)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 Mouse Apo-C3. 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 Mouse Apo-C3 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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