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Expression of cell surface IFN-γRα chains by BALB/c splenic lymphocytes. BALB/c spleen cells (including erythrocytes) were preincubated (~15 minutes, 4°C) with purified 2.4G2 antibody [BD Fc Block™; Cat. No. 553141/553142; 1 µg antibody/10e6 cells]. The cells were stained (30 minutes, 4°C) with purified 2E2 antibody (0.5 µg mAb/10e6 cells; Cat. No. 559911). After washing, the cells were incubated (30 minutes, 4°C) with a biotin-conjugated cocktail of mouse anti-hamster antibodies (Clones G70-204 + G94-56; cat. No. 554010; 0.5 µg mAb cocktail/10e6 cells). Finally, the cells were washed and incubated with R-PE-conjugated Streptavidin (Cat. No. 554061; 0.015 µg PE-SA/10e6 cells) and FITC-anti-CD4 (clone RM4-5; Cat. No. 553047) and FITC-anti-CD8 (clone 53-6.7; Cat. No. 553031), both at 0.06 µg mAb/10e6 cells. After washing, the cells were analyzed with a FACScan™ Flow Cytometer. The immunofluorescent staining patterns for erythrocytes and lymphocytes that were either not stained with 2E2 (top images, background staining) or were stained with purified 2E2 (bottom images) followed by the 2nd and 3rd layer reagents shown at right. The two-color dot plots were generated by gating for cells that had the light-scattering characteristics of erythrocytes (left images) or lymphocytes (right images). The data indicates that mouse erythrocytes are uniformly negative for IFN-γRα expression whereas most T cells (i.e., CD4+/CD8+ cells) and CD4-CD8- lymphocytes constitutively express medium levels of IFN-γRα chains.
BD Pharmingen™ Purified Hamster Anti-Mouse CD119
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Immunofluorescent Staining and Flow Cytometric Analysis: The purified form of 2E2 (Cat. No. 559911) can be used for the immunofluorescent staining (≤ 1 µg antibody/10e6 cells) and flow cytometric analysis of normal mouse cells or cell lines to measure their expressed levels of IFN-γRα. An appropriate purified immunoglobulin isotype control is A19-3. A three-layer staining protocol is recommended for maximizing the detection IFN-γRα chains expressed by cells as detailed in the figure legend.
Note: 2E2 is a nonblocking antibody that can be used for the unobstructed immunofluorescent staining and flow cytometric analysis of cells in systems where the ligand (i.e., IFN-γ) for IFN-γ receptors is present.
Immunoprecipitation: The 2E2 antibody has been reported to be useful for the immunoprecipitation of IFN-γRα chains from lysates of cloned mouse T cells.
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The 2E2 antibody recognizes the extracellular region of the 90 kDa alpha chain subunit of the mouse interferon-γ receptor (IFN-γRα; aka, CD119). The functionally active-form of the mouse IFN-γ receptor consists of two (or more) subunits, with IFN-γRα responsible for IFN-γ binding and both the IFN-γRα and IFN-γRβ chains required for the transduction of biologic responses. IFN-γRα is expressed by a variety of cell lines and normal mouse cells (except mature erythrocytes) including T cells, B cells, NK cells, monocytes, neutrophils, fibroblasts, epithelial and endothelial cells. The 2E2 antibody is a non-neutralizing antibody; it does not block the binding of IFN-γ to its receptor. The immunogen used to generate this hybridoma was a purified preparation of soluble recombinant mouse IFN-γRα chain protein.
研发参考 (1)
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Bach EA, Szabo SJ, Dighe AS, et al. Ligand-induced autoregulation of IFN-gamma receptor beta chain expression in T helper cell subsets.. Science. 1995; 270(5239):1215-8. (Clone-specific: Immunoprecipitation). 查看参考
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