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- 详细信息
- 文献和实验
- 技术资料
- 库存:
100
- 供应商:
艾美捷科技
- 应用:
说明书
- 适应物种:
说明书
- 标记物:
说明书
- 规格:
96T
关键词:人X-Box结合蛋白1(XBP1)CLIA试剂盒,Human X-Box Binding Protein 1 (XBP1) CLIA Kit,Human X-Box Binding Protein 1 (XBP1) CLIA Kit,人X-Box结合蛋白1(XBP1)CLIA试剂盒,Biomatik
产品名称:人X-Box结合蛋白1(XBP1)CLIA试剂盒-Human X-Box Binding Protein 1 (XBP1) CLIA Kit
产品货号:EKU10003
产品规格:96T
背景资料:This assay has high sensitivity and excellent specificity for detection of X-Box Binding Protein 1 (XBP1). No significant cross-reactivity or interference between X-Box Binding Protein 1 (XBP1) and analogues was observed.
保存建议:人X-Box结合蛋白1(XBP1)CLIA试剂盒-Human X-Box Binding Protein 1 (XBP1) CLIA KitBiomatik品牌厂家建议该人X-Box结合蛋白1(XBP1)CLIA试剂盒产品,Short term: 4°C; Long term: see manual.
产品描述: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 Fibroblast Growth Factor 2, Basic (FGF2). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Fibroblast Growth Factor 2, Basic (FGF2). 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 Fibroblast Growth Factor 2, Basic (FGF2), 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 Fibroblast Growth Factor 2, Basic (FGF2) in the samples is then determined by comparing the O.D. of the samples to the standard curve.
点击:人X-Box结合蛋白1(XBP1)CLIA试剂盒-Human X-Box Binding Protein 1 (XBP1) CLIA Kit查看更详细产品说明,更多应用、储存、价格、货期等信息请致电垂询艾美捷科技有限公司。更多Biomatik公司特色试剂盒、特色抗体以及特色试剂等产品评论,请点击查看艾美捷特色产品中心。
Biomatik公司于2002年在加拿大成立,是生物试剂一站式购物中心,提供29000+ELISA试剂盒,27000+抗体,17000+重组蛋白,280+生物试剂。除了目录产品外,Biomatik还为全球的研究人员提供62,000多种定制产品,包括基因合成、多肽合成、蛋白及抗体生产的定制服务。
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-freezing matrix. Block endogenous peroxidase activity by incubating the slides in 0.3% H2 O2 solution in PBS for 10 minutes. Rinse slides 3x in PBS, 2 minutes each time. Block non-specific binding by incubating with blocking buffer (10
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