详细说明
概述
产品名称Anti-Bad抗体[Y208]
描述
兔单克隆抗体[Y208] to Bad
特异性The antibody does not cross-react with other Bcl-2 members.
经测试应用WB,IHC-P,ICC/IF,Flow Cyt,IP
种属反应性
与反应: Mouse, Rat, Dog, Human
免疫原
A synthetic peptide corresponding to residues in the N-term of human Bad.
阳性对照
Hela cell lysate, human lymphoma.
常规说明
This product is a recombinant rabbit monoclonal antibody.
Produced using Abcam’s RabMAb® technology. RabMAb® technology is covered by the following U.S. Patents, No. 5,675,063 and/or 7,429,487.
Alternative versions available:
性能
形式Liquid
存放说明Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C. Avoid freeze / thaw cycle.
存储溶液PBS 49%,Sodium azide 0.01%,Glycerol 50%,BSA 0.05%
纯度Protein A purified
克隆单克隆
克隆编号Y208
同种型IgG
研究领域
Cancer
Cell Death
Apoptosis
Metabolism
Cancer
Cell Death
Apoptosis
Apoptotic Markers
Bcl 2 family
Metabolism
Pathways and Processes
Metabolism processes
Apoptosis
Cancer
Invasion/microenvironment
Apoptosis
Bcl 2 family
Cell Biology
Apoptosis
Intracellular
Bcl2 Family
Anti-Bad antibody [Y208] 图像
Western blot - Bad antibody [Y208] (ab32445)
Anti-Bad antibody [Y208] (ab32445) at 1/5000 dilution + Hela cell lysate
Predicted band size : 18 kDa
Observed band size : 23 kDa (why is the actual band size different from the predicted?)
Immunohistochemistry (Paraffin-embedded sections) - Bad antibody [Y208] (ab32445)
Immunohistochemical staining of paraffin-embedded human lymphoma using ab32445 at 1/100 dilution.
Immunocytochemistry/ Immunofluorescence-Bad antibody [Y208](ab32445)
ICC/IF image of ab32445 stained MCF7 cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab32445, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
Flow Cytometry-Bad antibody [Y208](ab32445)
Overlay histogram showing MCF-7 cells stained with ab32445 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab32445, 1/20 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (ab96899) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit monoclonal IgG (1µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a decreased signal in MCF-7 cells fixed with methanol (5 min)/permeabilized in 0.1% PBS-Tween used under the same conditions.