
563685 ·
BDB Bioscience · Cat: 563685
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bdbiosciences.com/en-us/products/reagents/flow-cytometry-rea...Description
Flow cytometric analysis of CD45.2 expression on C57BL/6 splenocytes. Splenic leucocytes from SJL mice Left Panel or C57BL/6 mice 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 BV711 Mouse IgG2a, kappa Isotype Control Cat. No. 563345; dashed line histogram or BD Horizon BV711 Mouse Anti-Mouse CD45.2 antibody Cat. No. 563685; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD45.2 expression on C57BL/6 splenocytes. Splenic leucocytes from SJL mice Left Panel or C57BL/6 mice 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 BV711 Mouse IgG2a, kappa Isotype Control Cat. No. 563345; dashed line histogram or BD Horizon BV711 Mouse Anti-Mouse CD45.2 antibody Cat. No. 563685; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD45.2 expression on C57BL/6 splenocytes. Splenic leucocytes from SJL mice Left Panel or C57BL/6 mice 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 BV711 Mouse IgG2a, kappa Isotype Control Cat. No. 563345; dashed line histogram or BD Horizon BV711 Mouse Anti-Mouse CD45.2 antibody Cat. No. 563685; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD45.2 expression on C57BL/6 splenocytes. Splenic leucocytes from SJL mice Left Panel or C57BL/6 mice 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 BV711 Mouse IgG2a, kappa Isotype Control Cat. No. 563345; dashed line histogram or BD Horizon BV711 Mouse Anti-Mouse CD45.2 antibody Cat. No. 563685; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD45.2 expression on C57BL/6 splenocytes. Splenic leucocytes from SJL mice Left Panel or C57BL/6 mice 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 BV711 Mouse IgG2a, kappa Isotype Control Cat. No. 563345; dashed line histogram or BD Horizon BV711 Mouse Anti-Mouse CD45.2 antibody Cat. No. 563685; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD45.2 expression on C57BL/6 splenocytes. Splenic leucocytes from SJL mice Left Panel or C57BL/6 mice 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 BV711 Mouse IgG2a, kappa Isotype Control Cat. No. 563345; dashed line histogram or BD Horizon BV711 Mouse Anti-Mouse CD45.2 antibody Cat. No. 563685; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System.