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。
核黄素激酶，也被称为RFK，由RFK基因编码的酶。在酶学中，它是一种催化化学反应的酶。该酶的两个底物是ATP和核黄素，而其两个产物是ADP和FMN。核黄素通过核黄素激酶的作用转化为催化活性辅因子（FAD和FMN），其腺苷化FMN为FAD。作为双功能酶一部分的细菌FAD合成酶与核苷酸转移酶具有遥远的相似性，因此，它可能参与FAD合成酶的腺苷酸化反应。 本试剂盒采用双抗体夹心法酶联免疫吸附试验（ELISA）。往预先包被有人核黄素激酶(RFK)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核黄素激酶(RFK)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 RFK. 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 RFK 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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