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。
白细胞介素23是一种由IL12B（IL-12p40）亚单位（与IL12共享）和IL23A（IL-23p19）亚单位组成的异质二聚体细胞因子。IL-23的功能性受体（IL-23受体）已被确定，由IL-12R β1和IL-23R组成。Adnectin-2与IL-23结合并与IL-23/IL-23R竞争。IL-23R在结合IL-23的域中有一些单核苷酸多态性，因此在激活Th17方面可能存在差异。IL-23已被证明是Th17维持和扩张的关键细胞因子。IL-6和TGF-β激活Th17转录因子RORγt，使Th17极化。IL-23稳定RORγt，从而使Th17能够正常运作并释放其效应细胞因子。 本试剂盒采用双抗体夹心法酶联免疫吸附试验（ELISA）。往预先包被有大鼠白细胞介素23(IL-23)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大鼠白细胞介素23(IL-23)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 Rat IL-23. 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 Rat IL-23 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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