Key features and details
- Mouse monoclonal [MEM-123] to HLA Class I
- Suitable for: ICC/IF, Flow Cyt
- Reacts with: Human, Monkey
- Isotype: IgG3
产品名称Anti-HLA Class I抗体[MEM-123]
参阅全部 HLA Class I 一抗
描述小鼠单克隆抗体[MEM-123] to HLA Class I
特异性This antibody reacts with all human classical MHC Class I molecules in native cell-surface forms as well as with human HLA-G cDNA transfected cells. This antibody completely blocks the binding of pan MHC antibody (ab7855) but does not block binding of anti-HLA-G(ab7758/7904) to surface-expressed HLA-G.
经测试应用适用于: ICC/IF, Flow Cytmore details
种属反应性与反应: Human, Monkey
Tissue/ cell preparation. COS-7 cells transfected with human CD48.
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存放说明Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
Preservative: 0.097% Sodium azide
Concentration information loading...
纯度Protein A purified
Our Abpromise guarantee covers the use of ab2217 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|ICC/IF||Use at an assay dependent concentration.|
|Flow Cyt||Use a concentration of 0.5 - 4 µg/ml.
ab91537 - Mouse monoclonal IgG3, is suitable for use as an isotype control with this antibody.
相关性HLA CLass I is involved in the presentation of foreign antigens to the immune system.
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Flow Cytometry analysis of human peripheral blood cells labeling HLA Class I with Anti-HLA Class I antibody [MEM-123] (ab2217).
ICC/IF image of ab2217 stained HeLa cells. The cells were 4% formaldehyde 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 (ab2217, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse 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.
Overlay histogram showing Jurkat cells stained with ab2217 (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 (ab2217, 0.5µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was mouse IgG3 [MG3-35] (ab18394, 1µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in Jurkat cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.