国产传媒国产福利9|亚洲www啪成人一区二区麻豆国产av一区二区凹凸精品|九色91欧美亚洲精品一区二三区|国产真实交换配乱吟91日韩高清带中文字幕|欧美精品中文字幕亚洲专区久久久精品国产自拍|国产在线观看91精品腿张开|糖心vlog免费版下载|国产精品久久久久久久久久99|色成人av|伊人中文字幕在线观看,糖心vlog是什么,久久精品国产亚洲av高潮,国产青草91精品免费

The Mouse Interleukin 12 (IL-12) p70 ELISA Kit is designed for the quantitative detection and measurement of mouse IL-12 (p70) in biological fluids such as serum, plasma, and cell culture supernatants. IL-12 (p70) is a heterodimeric cytokine composed of p35 and p40 subunits; the p40 subunit is shared with IL-23. IL-12 is produced by monocytes, macrophages, dendritic cells, neutrophils, and B cells. IL-12 is a regulator of cytokine synthesis, especially IFN-γ, enhances the proliferation of T and NK cells, and stimulates the differentiation of CD4+ and CD8+ T cells. The assay is based on the sandwich ELISA method, in which samples are added to ELISA strip plates pre-coated with capture antibodies specific for the cytokine. The captured cytokine is detected by addition of a biotinylated detection antibody, followed by streptavidin-horseradish peroxidase, which binds the biotinylated antibody. Addition of the chromogenic enzyme substrate 3,3’,5,5’ tetramethylbenzidine (TMB) results in a colored product with an intensity directly proportional to the concentration of cytokine in the sample. The concentration of the cytokine is determined by comparison to a serial dilution of the cytokine standard analyzed in parallel.