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转化生长因子β1(TGF-b1)酶联免疫吸附检测试剂盒(需活化)
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品牌 科鹿
地区 中国,湖北省
货号 ELK10034
产地 国产
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96T
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科鹿生物
科鹿(武汉)生物科技有限责任公司
武汉东湖新技术开发区高科园三路9号武汉光谷精准医疗产业基地2.1期11栋203号房
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科鹿(武汉)生物科技有限责任公司位于武汉精准医疗产业基地2.1期11栋。成立于2018年,是一家专业从事生命科学和免疫研究的高科技生物企业。公司拥有6000平方米的实验室,拥有独立的细胞培养室和SPF动物室,专业从事形态病理学、细胞生物学、分子生物学、蛋白质免疫学、模型动物相关产品的引进和研发。公司成立以来,团队成员参与了多项医学生物学研究项目和国家自然科学基金项目。集研发、生产、营销一体化全球化试剂供应商,并与全国多家企业和科研机构建立合作关系,为每一位科研人员提供最优质、最高效的服务和产品。
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产品规格 图文详情 技术文档
产品规格
品牌名称
科鹿
货号
ELK10034
国产/进口
国产
规格
96T
货源
新品
图文详情
Product name:TGF-b1(TransformingGrowth Factor Beta 1) ELISA Kit(Activation Required)
Reactivity:General
Alternative Names:Cartilage-inducing factor,CED,Differentiation inhibiting factor,DPD1,LAP,Latency-associated peptide,Prepro transforming growth factor beta 1,TGF beta 1,TGF beta,TGF beta 1 protein,TGF-beta 1 protein,TGF-beta-1,TGF-beta-5,TGF-beta1,TGFB,Tgfb-1,tgfb1,TGFB1,TGFbeta,TGFbeta1,Transforming Growth Factor b1,Transforming Growth Factor beta 1,Transforming growth factor beta 1a,transforming growth factor beta-1,transforming growth factor,beta 1,Transforming Growth Factor-ß1
Assay Type:Sandwich
Sensitivity:0.11 ng/mL
Standard:10 ng/mL
Detection Range:0.16-10 ng/mL
Sample Type:Activated serum, plasma
Assay Length:3.5h
Research Area:Cytokine;Tumor immunity;Infection immunity;
Test principle:The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to TGF-b1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to TGF-b1. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain TGF-b1, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of TGF-b1 in the samples is then determined by comparing the OD of the samples to the standard curve.
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