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。
SKI样癌基因（SKIL），也被称为SNOA或SNO，是由SKIL基因编码的蛋白质。SKIL属于Ski/Sno/Dac家族，由SKI蛋白、Dachshund和SKIDA1共享。Ski/Sno/Dac家族的成员共享一个大约100个氨基酸长的域。它可能在响应细胞外信号的细胞分裂或分化中具有调节作用。它已被证明可以激活肌肉特异性基因的表达。它还调节神经元细胞功能，例如作为轴突生长的有效启动子。它可能参与T细胞功能的调节。它是通过其与Smad蛋白相互作用和抑制活性的能力来转化生长因子β信号传导的重要负调节因子。 本试剂盒采用双抗体夹心法酶联免疫吸附试验（ELISA）。往预先包被有人SKI样癌基因(SKIL)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SKI样癌基因(SKIL)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 SKIL. 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 SKIL 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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