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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。
鞘氨醇1磷酸酯裂解酶1,也被称为SGPL1,是由SGPL1基因编码的酶。它将磷酸化鞘氨醇碱基 (PSB)(例如 1-磷酸鞘氨醇)裂解为脂肪醛和磷酸乙醇胺。它提高应激诱导的神经酰胺产生和细胞凋亡。它是肝脏中的整体脂质稳态和成纤维细胞中的胆固醇稳态所必需的。它参与调节促炎反应和中性粒细胞运输。它通过磷酸乙醇胺的产生调节神经元自噬,磷酸乙醇胺调节易于聚集的蛋白质(如 APP)的积累。它似乎在建立神经元接触位点和轴突维护方面发挥作用。SGPL1缺乏症会引发大脑中易聚集蛋白的积累和认知缺陷。 本试剂盒采用双抗体夹心法酶联免疫吸附试验(ELISA)。往预先包被有小鼠鞘氨醇1磷酸酯裂解酶1(SGPL1)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鞘氨醇1磷酸酯裂解酶1(SGPL1)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 SGPL1. 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 SGPL1 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.