分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材
Pro-Apoptotic WT1 Regulator Recombinant Rabbit mAb [KD验证]
分享
收藏
产品详情
FAQ
产品文档
已发表文献
推荐应用
产品介绍
This gene encodes a tumor suppressor protein that selectively induces apoptosis in cancer cells through intracellular and extracellular mechanisms. The intracellular mechanism involves the inhibition of pro-survival pathways and the activation of Fas-mediated apoptosis, while the extracellular mechanism involves the binding of a secreted form of this protein to glucose regulated protein 78 (GRP78) on the cell surface, which leads to activation of the extrinsic apoptotic pathway. This gene is located on the unstable human chromosomal 12q21 region and is often deleted or mutated different tumors. The encoded protein also plays an important role in the progression of age-related diseases.
产品性质
产品特色
推荐稀释比 WB: 1/1000-1/5000; FC: 1/200-1/2000; ICC/IF: 1/100-1/1000
应用案例

本产品仅用作科学研究!


Immunocytochemical staining of HeLa cells using PAWR antibody , Top panel: wild-type (WT); Bottom panal: PAWR shRNA knockdown (KD). Nuclei were stained blue with DAPI; PAWR was stained magenta with Alexa Fluor® 647. Scale bar, 20 μm. Permeabilization: Triton.

Flow cytometric analysis of PAWR expression in HepG2 cells using PAWR antibody . Green, isotype control; red, PAWR.

Immunocytochemical staining of HepG2 cells with PAWR antibody . Nuclei were stained blue with DAPI; PAWR was stained magenta with Alexa Fluor® 647. Images were taken using Leica stellaris 5. Protein abundance based on laser Intensity and smart gain: Medium. Scale bar, 20 μm.

Western blotting analysis using PAWR antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with PAWR antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using FeQ™ ECL Substrate Kit .

Western blotting analysis using PAWR antibody . PAWR expression in wild-type (WT) and PAWR shRNA knockdown (KD) HeLa cells with 20 μg of total cell lysates. Hsp90 α serves as a loading control. The blot was incubated with PAWR antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using NaQ™ ECL Substrate Kit .

Validation of PAWR knockdown using flow cytometry. Wild-type(WT, Blue) and knockdown(KD, Green) HeLa cells were stained with PAWR antibody and analyzed using BD flow cytometer.

存储条件
Store at -20℃ for one year.
COA
已发表文献
联系我们
购物车
客服
转染试用