计算溶液所需的质量、体积或浓度。
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。
核因子κB受体活化因子(RANK),又称TRANCE受体或TNFRSF11A,是肿瘤坏死因子受体(TNFR)分子亚家族的一员。RANK是RANK-配体(RANKL)的受体,是调节破骨细胞分化和激活的RANK/RANKL/OPG信号传导途径的一部分。骨保护素(OPG)是RANKL的诱饵受体,并通过竞争RANKL来调节RANK信号通路的刺激。RANK的细胞质结构域与TRAFs 1、2、3、5和6结合,将信号传递给下游目标,如NF-κB和JNK。RANK是一个616个氨基酸的I型跨膜蛋白。它的细胞外结构域由184个氨基酸组成,其跨膜结构域有21个氨基酸,其细胞质结构域由383个氨基酸组成。 本试剂盒采用双抗体夹心法酶联免疫吸附试验(ELISA)。往预先包被有小鼠核因子κB受体活化因子(RANK)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核因子κB受体活化因子(RANK)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 RANK. 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 RANK 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.