BD PharmingenTM APC-H7 Rat Anti-Mouse Ly-6G

Description

Multiparameter flow cytometric analysis of Ly-6G expression on mouse bone-marrow leucocytes. Mouse bone-marrow cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with either APC-H7 Rat IgG2a, kappa Isotype Control Cat. No. 560197; dashed line histogram or APC-H7 Rat Anti-Mouse LY-6G antibody Cat. No. 565369; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphoid Left Panel or myeloid Right Panel bone marrow leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Multiparameter flow cytometric analysis of Ly-6G expression on mouse bone-marrow leucocytes. Mouse bone-marrow cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with either APC-H7 Rat IgG2a, kappa Isotype Control Cat. No. 560197; dashed line histogram or APC-H7 Rat Anti-Mouse LY-6G antibody Cat. No. 565369; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphoid Left Panel or myeloid Right Panel bone marrow leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Multiparameter flow cytometric analysis of Ly-6G expression on mouse bone-marrow leucocytes. Mouse bone-marrow cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with either APC-H7 Rat IgG2a, kappa Isotype Control Cat. No. 560197; dashed line histogram or APC-H7 Rat Anti-Mouse LY-6G antibody Cat. No. 565369; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphoid Left Panel or myeloid Right Panel bone marrow leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Show More Multiparameter flow cytometric analysis of Ly-6G expression on mouse bone-marrow leucocytes. Mouse bone-marrow cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with either APC-H7 Rat IgG2a, kappa Isotype Control Cat. No. 560197; dashed line histogram or APC-H7 Rat Anti-Mouse LY-6G antibody Cat. No. 565369; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphoid Left Panel or myeloid Right Panel bone marrow leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Show More Multiparameter flow cytometric analysis of Ly-6G expression on mouse bone-marrow leucocytes. Mouse bone-marrow cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with either APC-H7 Rat IgG2a, kappa Isotype Control Cat. No. 560197; dashed line histogram or APC-H7 Rat Anti-Mouse LY-6G antibody Cat. No. 565369; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphoid Left Panel or myeloid Right Panel bone marrow leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Multiparameter flow cytometric analysis of Ly-6G expression on mouse bone-marrow leucocytes. Mouse bone-marrow cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody Mouse BD Fc Block Cat. No. 553141/553142 . The cells were then stained with either APC-H7 Rat IgG2a, kappa Isotype Control Cat. No. 560197; dashed line histogram or APC-H7 Rat Anti-Mouse LY-6G antibody Cat. No. 565369; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphoid Left Panel or myeloid Right Panel bone marrow leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System.