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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
详见官方网站
- 亚型:
详见官方网站
- 形态:
冻干粉/浓缩液
- 保存条件:
-20℃
- 克隆性:
多克隆
- 标记物:
详见说明书
- 适应物种:
详见说明书
- 宿主:
详见官方网站
- 应用范围:
详见官方网站
- 浓度:
1mg/ml
- 抗体英文名:
N-acetyl-β-D-glucosaminidase (NAG) Assay (Three vial liquid stable) (Colorimetric)
- 规格:
100ug,200ug,1mg
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文献和实验Scintillation Proximity Assay (SPA) Technology to Study Biomolecular Interactions
demonstration of an intermolecular SH2‐phosphotyrosine interaction in the Crk protein. Cell. 80:237‐248. Cook, N.D. 1996. Scintillation proximity assay: A versatile high‐throughput
andperform a β-catenin immunoblot as recommended by manufacturer. An example of this β-catenin stabilization assay isshown in Fig. 2.3 . 4. Notes 1. This purification can be applied to other Wnt proteins: to date,Wnt3A, 5A, 7A, 16, Wingless, and Dwnt
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
. The following protocol willyield high-titer virus that can be used to generate stable reportercell lines, assay Wnt/b-catenin signaling in cells that are difficultto transfect such as primary cultures, or assay signaling in vivo. BAR and fuBAR virus
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