BD HorizonTM BUV395 Rat Anti-Mouse Ly-6G

Description

Flow cytometric analysis of Ly-6G expression on mouse bone-marrow leukocytes. 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 BD Horizon BUV395 Rat IgG2a, kappa Isotype Control Cat. No. 563556; dashed line histogram or BD Horizon BUV395 Rat Anti-Mouse LY-6G antibody Cat. No. 563978/565964; solid line histogram . The fluorescence histograms were derived from gated events with the light scattering characteristics of viable lymphoid Left Panel or myeloid Right Panel cells. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of Ly-6G expression on mouse bone-marrow leukocytes. 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 BD Horizon BUV395 Rat IgG2a, kappa Isotype Control Cat. No. 563556; dashed line histogram or BD Horizon BUV395 Rat Anti-Mouse LY-6G antibody Cat. No. 563978/565964; solid line histogram . The fluorescence histograms were derived from gated events with the light scattering characteristics of viable lymphoid Left Panel or myeloid Right Panel cells. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of Ly-6G expression on mouse bone-marrow leukocytes. 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 BD Horizon BUV395 Rat IgG2a, kappa Isotype Control Cat. No. 563556; dashed line histogram or BD Horizon BUV395 Rat Anti-Mouse LY-6G antibody Cat. No. 563978/565964; solid line histogram . The fluorescence histograms were derived from gated events with the light scattering characteristics of viable lymphoid Left Panel or myeloid Right Panel cells. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of Ly-6G expression on mouse bone-marrow leukocytes. 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 BD Horizon BUV395 Rat IgG2a, kappa Isotype Control Cat. No. 563556; dashed line histogram or BD Horizon BUV395 Rat Anti-Mouse LY-6G antibody Cat. No. 563978/565964; solid line histogram . The fluorescence histograms were derived from gated events with the light scattering characteristics of viable lymphoid Left Panel or myeloid Right Panel cells. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of Ly-6G expression on mouse bone-marrow leukocytes. 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 BD Horizon BUV395 Rat IgG2a, kappa Isotype Control Cat. No. 563556; dashed line histogram or BD Horizon BUV395 Rat Anti-Mouse LY-6G antibody Cat. No. 563978/565964; solid line histogram . The fluorescence histograms were derived from gated events with the light scattering characteristics of viable lymphoid Left Panel or myeloid Right Panel cells. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of Ly-6G expression on mouse bone-marrow leukocytes. 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 BD Horizon BUV395 Rat IgG2a, kappa Isotype Control Cat. No. 563556; dashed line histogram or BD Horizon BUV395 Rat Anti-Mouse LY-6G antibody Cat. No. 563978/565964; solid line histogram . The fluorescence histograms were derived from gated events with the light scattering characteristics of viable lymphoid Left Panel or myeloid Right Panel cells. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System.