BD PharmingenTM FITC Rat Anti-Mouse T- and B-Cell Activation Antigen

Description

Flow cytometric analysis for T- and B- Cell Activation Antigen in activated mouse spleen cells. Concanavalin A-stimulated 3 days mouse splenic leucocytes 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 FITC Rat IgM, kappa Isotype Control Cat No. 553942; dashed line histogram or with the FITC Rat Anti-Mouse T- and B- Cell Activation Antigen antibody Cat No. 553666/562080; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphoblasts. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Flow cytometric analysis for T- and B- Cell Activation Antigen in activated mouse spleen cells. Concanavalin A-stimulated 3 days mouse splenic leucocytes 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 FITC Rat IgM, kappa Isotype Control Cat No. 553942; dashed line histogram or with the FITC Rat Anti-Mouse T- and B- Cell Activation Antigen antibody Cat No. 553666/562080; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphoblasts. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Show More Flow cytometric analysis for T- and B- Cell Activation Antigen in activated mouse spleen cells. Concanavalin A-stimulated 3 days mouse splenic leucocytes 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 FITC Rat IgM, kappa Isotype Control Cat No. 553942; dashed line histogram or with the FITC Rat Anti-Mouse T- and B- Cell Activation Antigen antibody Cat No. 553666/562080; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphoblasts. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System.