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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
天然和重组IL-12和IL-23的p40亚基
- 抗体英文名:
anti-human IL-12/-23 (p40) mAbs MT86/221, purified
- 规格:
250ug
产品名称:anti-human IL-12/-23 (p40) mAbs MT86/221, purified-anti-human IL-12/-23 (p40) mAbs MT86/221, purified
产品货号:3450-3-250 产品规格:250ug 应用类型:ELISpot, ELISA
保存建议:anti-human IL-12/-23 (p40) mAbs MT86/221, purified-anti-human IL-12/-23 (p40) mAbs MT86/221, purified建议收到产品后2-8°C保存,有效期为18个月。
背景资料:Interleukin-12 (IL-12, IL12) is, when biologically active, a heterodimer (p70) consisting of two covalently linked subunits, p35 and p40. IL-12 is produced by antigen-presenting cells, specifically dendritic cells and macrophages. IL-12 is a proinflammatory cytokine that promotes Th1-type responses by inducing IFN-γ production and enhancing proliferation and cytotoxicity of NK and T cells. Interleukin-23 (IL-23) is a disulfide-linked heterodimer which consists of a unique p19 subunit and the p40 subunit of IL-12. IL-23 is a proinflammatory cytokine, which is produced by macrophages and dendritic cells upon infections with certain pathogens. The IL-23 receptor is expressed on Th17 cells and IL-23 is responsible for Th17 expansion and stabilization. Since both IL-12 and IL-23 heterodimers comprise the p40 subunit, capture immunoassays based on antibodies to p40 will detect both cytokines. Such assays can also detect p40 monomers and dimers.
点击:anti-human IL-12/-23 (p40) mAbs MT86/221, purified-anti-human IL-12/-23 (p40) mAbs MT86/221, purified查看更详细产品说明,更多应用、储存、价格、货期等信息请致电400-6800-868垂询Mabtech中国区域授权总代理艾美捷科技有限公司。更多特色试剂盒、特色抗体以及特色试剂等产品评论,请点击查看每日生物评论网站。
Mabtech 公司是一家欧洲的集研究,开发,销售,技术支持为一体的高科技免疫生物技术公司。Mabtech公司始终专业致力于研发新的单克隆抗体,生产创新的免疫试剂和销售高品质的全配套的免疫试剂盒。公司核心业务是致力于优化发展酶联免疫斑点法技术 (ELISpot)、荧光免疫斑点法技术 (FluoroSpot) 和酶联免疫吸附试验技术 (ELISA) 等免疫学方法。作为Mabtech在中国的区域代理,艾美捷科技有限公司将为中国客户提供全面的Mabtech产品以及客户订制化服务。
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关键词:anti-human IL-12/-23 (p40) mAbs MT86/221, purified,anti-human IL-12/-23 (p40) mAbs MT86/221, purified, IL-12/-23(p40)mAbs MT86/221
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microRNA detection platform to identify genes that are induced by IFNα in hepatoma- or melanoma-derived human tumor cell lines. Despite the enormous differences in expression levels between these models, we were able to identify microRNAs
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