详细说明
概述
产品名称Anti-Ku70抗体[EPR4027]
描述
兔单克隆抗体[EPR4027] to Ku70
经测试应用WB,IP,IHC-P,Flow Cyt,ICC/IF
种属反应性
与反应: Human
免疫原
A synthetic peptide corresponding to residues in Human Ku70
阳性对照
HeLa, 293T, A549 and A431 cell lysates. Human testis tissue, Human tonsil tissue.
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.
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species. Please contact us for more information.
Alternative versions available:
Anti-Ku70 antibody (Alexa Fluor® 488) [EPR4027] (ab199225)
Anti-Ku70 antibody (Alexa Fluor® 647) [EPR4027] (ab199458)
性能
形式Liquid
存放说明Shipped at 4°C. Store at -20°C. Stable for 12 months at -20°C.
存储溶液PBS 49%,Sodium azide 0.01%,Glycerol 50%,BSA 0.05%
纯度Tissue culture supernatant
克隆单克隆
克隆编号EPR4027
同种型IgG
研究领域
Cancer
Cell cycle
Cell division
Epigenetics and Nuclear Signaling
DNA / RNA
DNA Damage & Repair
Non Homol. End Joining
Anti-Ku70 antibody [EPR4027] 图像
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Ku70 antibody [EPR4027] (ab92450)
Paraffin embedded Human testis tissue (A) or Human tonsil tissue (B) were labelled with ab92450 at 1/100 dilution.
Western blot - Ku70 antibody [EPR4027] (ab92450)
All lanes : Anti-Ku70 antibody [EPR4027] (ab92450) at 1/1000 dilution
Lane 1 : HeLa cell lysate
Lane 2 : 293T cell lysate
Lane 3 : A549 cell lysate
Lane 4 : A431 cell lysate
Lysates/proteins at 10 µg per lane.
Secondary
HRP labelled goat anti-rabbit at 1/2000 dilution
Predicted band size : 70 kDa
Immunocytochemistry/ Immunofluorescence - Ku70 antibody [EPR4027] (ab92450)
Immunofluorescence staining of HeLa cells using ab92450 at 1/100 dilution.
Flow Cytometry-Anti-Ku70 antibody [EPR4027](ab92450)
Overlay histogram showing HeLa cells stained with ab92450 (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 (ab92450, 1/100 dilution) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (ab96899) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was rabbit IgG (monoclonal) (1µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HeLa cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.