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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。
骨成型蛋白7(BMP-7)是一种蛋白质,由BMP7基因编码。该基因所编码的蛋白是TGF-β超家族的成员。与骨形态发生蛋白家族的其他成员一样,它在间质细胞转化为骨和软骨的过程中起着关键作用。它被noggin和一种类似的蛋白chordin所抑制,后者在Spemann-Mangold Organizer中表达。BMP7可能参与骨的稳态,它在大脑、肾脏和膀胱中表达。BMP7诱导SMAD1和SMAD5的磷酸化,进而诱导众多成骨基因的转录。 本试剂盒采用双抗体夹心法酶联免疫吸附试验(ELISA)。往预先包被有大鼠骨成型蛋白7(BMP7)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骨成型蛋白7(BMP7)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 BMP7. 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 BMP7 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.