BD HorizonTM BUV395 Rat Anti-Mouse Ly-6A/E

Description

Flow cytometric analysis of Ly-6A/E expression on activated mouse splenocytes. Concanavlin A-activated BALB/c mouse splenocytes 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-6A/E antibody Cat. No. 563990, solid line histogram . Fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable activated splenocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of Ly-6A/E expression on activated mouse splenocytes. Concanavlin A-activated BALB/c mouse splenocytes 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-6A/E antibody Cat. No. 563990, solid line histogram . Fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable activated splenocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of Ly-6A/E expression on activated mouse splenocytes. Concanavlin A-activated BALB/c mouse splenocytes 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-6A/E antibody Cat. No. 563990, solid line histogram . Fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable activated splenocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System.