Es gibt 1 Publikation für dieses Produkt. Der Armenischer Hamster Monoklonal anti-IFNGR1 Antikörper wird verwendet zum Nachweis von IFNGR1 in Proben von Maus. Er wurde validiert für FACS.
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. This antibody is routinely tested by flow cytometric analysis. Other applications were tested during antibody development only or reported in the literature. Expression of cell surface IFN-γRα by BALB/c splenic lymphocytes. RBC-lysed BALB/c spleen cells were preincubated (~15 minutes, 4 °C) with purified 2.4G2 antibody [rat anti-mouse CD16 (FcγIII)/CD32 (FcγII), Cat. No. 553142, 1 μg antibody/10e6 cells]. The cells were stained (30 minutes, 4 °C) with biotinylated 2E2 antibody (1 μg mAb/10e6 cells, Cat. No. 550482) followed by R-PE-conjugated streptavidin (Cat. No. 554061, 0.015 μg PE-SA/10e6 cells). After washing, the cells were analyzed with a FACScan™ Flow Cytometer. The immunofluorescent staining patterns for cells stained with either biotinylated 2E2 antibody (filled histogram) or Streptavidin-PE (background staining, empty histogram) are shown. The histograms were generated from reanalyzed flow cytometric data files that were gated for events with the light-scattering characteristics of lymphocytes.