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。
神经胶质纤维酸性蛋白(GFAP)是一种由GFAP基因编码的蛋白质。它是一种III型中间丝（IF）蛋白，由中枢神经系统（CNS）的许多细胞类型表达，包括星形胶质细胞和发育期的上皮细胞。它与其他三个非上皮的III型IF家族成员--波形蛋白、去甲蛋白和周边蛋白密切相关，它们都参与了细胞骨架的结构和功能。它被认为有助于维持星形胶质细胞的机械强度以及细胞的形状。该蛋白由Lawrence F. Eng于1969年命名，并首次对其进行分离和定性。 本试剂盒采用双抗体夹心法酶联免疫吸附试验（ELISA）。往预先包被有小鼠神经胶质纤维酸性蛋白(GFAP)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小鼠神经胶质纤维酸性蛋白(GFAP)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 Mouse GFAP. 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 Mouse GFAP 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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