- ￥2890
- LSM Bio
- 0.15-10NG/ML
- 0.078NG/ML
- 进口
- EF006693
- 2025年07月13日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
50
- 供应商：
LSMBIO
- 检测范围：
0.15-10NG/ML
- 检测方法：
夹心法
- 应用：
夹心法ELISA体外定量检测人血清、血浆或其它相关生物液体中蛋白浓度
- 适应物种：
人
- 标记物：
Human Alpha E catenin
- 样本：
人血清、血浆或其它相关生物液体中天然和重组蛋白
- 灵敏度：
0.078NG/ML
- 规格：
96T
Alpha E catenin ELISA KIT|Human
Catalog EF006693
Packing 48T/96T
Reactivity Human
Detect Range 0.156-10ng/ml
Alpha E catenin ELISA KIT Sensitivity< 0.094ng/ml
Application Alpha E catenin ELISA KIT|Human is for detecting the concentration of Human Alpha E catenin in serum, plasma, tissue homogenates and other biological fluids.
Storage condition 6 month at 4 Centigrade
Principle of Alpha E catenin ELISA KIT|Human
The microtiter plate provided in Alpha E catenin ELISA KIT|Human has been pre-coated with an Human Alpha E catenin antibody specific to Human Alpha E catenin. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated Human Alpha E cateninantibody preparation specific for Human Alpha E catenin then avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain Human Alpha E catenin, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm . The concentration of Human Alpha E cateninin the samples is then determined by comparing the O.D. of the samples to the standard curve.
*Please noted that Alpha E catenin ELISA KIT|Human is only for RUO (Research Use Only), Not for the diagnostic Purpose!
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Control Interferon-alpha treated
v468.Chapter 8 采用 b-Catenin/TCF基本转录通讯结构对b-Catenin/TCF转录进行分析
1181. 9. Olson, L.E., Tollkuhn, J., Scafoglio, C., Krones, A., Zhang, J., Ohgi, K.A., Wu, W., Taketo, M.M., Kemler, R., Grosschedl, R., et al. (2006). Homeodomain-mediated beta-catenin-dependent switching events dictate cell-lineage determination
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