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。
黄嘌呤氧化酶(XO 或 XAO)是黄嘌呤氧化还原酶的一种形式,黄嘌呤氧化还原酶是一种产生活性氧的酶。这些酶催化次黄嘌呤氧化成黄嘌呤,并可以进一步催化黄嘌呤氧化成尿酸。黄嘌呤氧化酶是一种产生超氧化物的酶,通常存在于血清和肺部,在甲型流感感染期间其活性增加。在严重肝损伤期间,黄嘌呤氧化酶会释放到血液中,因此 XO 血液检测是确定是否发生肝损伤的一种方法。 本试剂盒采用双抗体夹心法酶联免疫吸附试验(ELISA)。往预先包被有大鼠黄嘌呤氧化酶(XOD)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黄嘌呤氧化酶(XOD)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 XOD. 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 XOD 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.