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。
易位关联膜蛋白1，也被称为TRAM1，由TRAM1基因编码。它通过促进在 SEC61通道的正确链定位，参与新生蛋白质链进入或通过内质网 (ER) 膜的易位。在易位到ER期间调节新生分泌蛋白链对胞质溶胶的暴露。可能影响 SEC61 通道侧门附近的磷脂双层，从而促进 ER 蛋白转运。在整个整合到 ER 膜的过程中，与新生膜蛋白的跨膜 (TM) 结构域密切相关。与ER膜中G 蛋白偶联受体视蛋白/OPSD新生链的第二个TM结构域相关，这可能有助于其整合到膜中。 本试剂盒采用双抗体夹心法酶联免疫吸附试验（ELISA）。往预先包被有人易位关联膜蛋白1(TRAM1)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易位关联膜蛋白1(TRAM1)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 TRAM1. 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 TRAM1 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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