- 询价
- 艾美捷代理Mabtech
- 3119-6-250
- 2025年07月07日
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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IFN-γ
- 抗体英文名：
anti-bovine IFN-gamma mAb MT307, biotinylated
- 规格：
250ug
产品名称：anti-bovine IFN-gamma mAb MT307, biotinylated-anti-bovine IFN-gamma mAb MT307, biotinylated
产品货号：3119-6-250 产品规格：250ug 应用类型：ELISpot, ELISA, FC
保存建议：anti-bovine IFN-gamma mAb MT307, biotinylated-anti-bovine IFN-gamma mAb MT307, biotinylated建议收到产品后2-8°C保存，有效期为18个月。
背景资料：Interferon-γ (IFN-γ, also known as IFN-gamma, IFN-g, IFNg and Interferon-gamma) is produced mainly by activated T cells and NK cells. It is a proinflammatory cytokine that activates macrophages and endothelial cells, but it also regulates immune responses by effecting APC and T and B cells. Production of IFN-γ by helper T cells as well as cytotoxic T cells is a hallmark of the TH1-type phenotype, thus, high-level production of IFN-γ is typically associated with effective host defense against intracellular pathogens.
点击：anti-bovine IFN-gamma mAb MT307, biotinylated-anti-bovine IFN-gamma mAb MT307, biotinylated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。
艾美捷科技有限公司品线覆盖生物研究各个领域，主要包括：分子生物学（核酸蛋白研究工具、cDNA/RNA、转染试剂、植物组培/细胞培养、生化试剂及试剂盒），试剂（蛋白酶抑制剂、化合物、荧光染料/探针、动物血清）、抗体（一抗、二抗、封闭血清）， 蛋白及试剂盒（细胞因子/重组蛋白、细胞凋亡/代谢/损伤、表观遗传、天然免疫）等。艾美捷为您寻找并提供最优的产品解决方案、最完备的物流服务、最及时的售后服务。如果您对上述产品线感兴趣，请致电免费服务热线到艾美捷垂询相关产品信息及完整实验解决方案。
关键词：anti-bovine IFN-gamma mAb MT307, biotinylated，anti-bovine IFN-gamma mAb MT307, biotinylated， IFN-gamma mAb MT307
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文献和实验Dual- and Triple-Color Fluorospot
, in PBS containing 0.1% bovine serum albumin (BSA) (seeNote 8). Add 100 μl/well and leave the plate for 2 h at room temperature. c. Wash the plate as in step 6 above. d. Dilute secondary detection reagents, i.e., mAb anti-FITC
Detection of apoptotic process in situ using immunocytochemical and TUNEL assays
antibody (mAb) conjugated with peroxidase (anti-DNA-POD) was used. This anti-DNA-POD mAb binds to single- and double-stranded, low molecular weight DNA fragments (mono- and oligonucleosomes), showing the internucleosomal degradation of genomic DNA occuring
Immunofluorescent Staining of Mouse and Rat Leukocytes
cold wash buffer (PBS/0.1% NaN3/1.0% fetal bovine serum). Centrifuge at 350 x g for 5 min. Finally, resuspend cell pellet to a concentration of 2 x 107 cells/ml (i.e., 106 cells per 50 µl). Dilute primary mAbs (e.g., unconjugated, biotinylated
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