BD HorizonTM BUV395 Mouse Anti-Mouse CD45.2

Description

Flow cytometric analysis of CD45.2 expression on C57BL/6 mouse splenocytes. Splenic leucocytes from an SJL mouse Left Panel or a C57BL/6 mouse Right Panel 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 Mouse IgG2a, kappa Isotype Control Cat. No. 563809; dashed line histogram or BD Horizon BUV395 Mouse Anti-Mouse CD45.2 antibody Cat. No. 564616; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD45.2 expression on C57BL/6 mouse splenocytes. Splenic leucocytes from an SJL mouse Left Panel or a C57BL/6 mouse Right Panel 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 Mouse IgG2a, kappa Isotype Control Cat. No. 563809; dashed line histogram or BD Horizon BUV395 Mouse Anti-Mouse CD45.2 antibody Cat. No. 564616; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD45.2 expression on C57BL/6 mouse splenocytes. Splenic leucocytes from an SJL mouse Left Panel or a C57BL/6 mouse Right Panel 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 Mouse IgG2a, kappa Isotype Control Cat. No. 563809; dashed line histogram or BD Horizon BUV395 Mouse Anti-Mouse CD45.2 antibody Cat. No. 564616; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD45.2 expression on C57BL/6 mouse splenocytes. Splenic leucocytes from an SJL mouse Left Panel or a C57BL/6 mouse Right Panel 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 Mouse IgG2a, kappa Isotype Control Cat. No. 563809; dashed line histogram or BD Horizon BUV395 Mouse Anti-Mouse CD45.2 antibody Cat. No. 564616; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD45.2 expression on C57BL/6 mouse splenocytes. Splenic leucocytes from an SJL mouse Left Panel or a C57BL/6 mouse Right Panel 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 Mouse IgG2a, kappa Isotype Control Cat. No. 563809; dashed line histogram or BD Horizon BUV395 Mouse Anti-Mouse CD45.2 antibody Cat. No. 564616; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD45.2 expression on C57BL/6 mouse splenocytes. Splenic leucocytes from an SJL mouse Left Panel or a C57BL/6 mouse Right Panel 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 Mouse IgG2a, kappa Isotype Control Cat. No. 563809; dashed line histogram or BD Horizon BUV395 Mouse Anti-Mouse CD45.2 antibody Cat. No. 564616; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System.