BD HorizonTM BV480 Rat Anti-Mouse CD44

Description

Flow cytometric analysis of CD44 expression on mouse bone-marrow cells. BALB/c 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 BV480 Rat IgG2b, kappa Isotype Control Cat. No. 565649; dashed line histogram or BD Horizon BV480 Rat Anti-Mouse CD44 antibody Cat. No. 566116/566200; solid line histogram . The fluorescence histogram showing CD44 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable bone marrow cells. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Flow cytometric analysis of CD44 expression on mouse bone-marrow cells. BALB/c 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 BV480 Rat IgG2b, kappa Isotype Control Cat. No. 565649; dashed line histogram or BD Horizon BV480 Rat Anti-Mouse CD44 antibody Cat. No. 566116/566200; solid line histogram . The fluorescence histogram showing CD44 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable bone marrow cells. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Show More Flow cytometric analysis of CD44 expression on mouse bone-marrow cells. BALB/c 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 BV480 Rat IgG2b, kappa Isotype Control Cat. No. 565649; dashed line histogram or BD Horizon BV480 Rat Anti-Mouse CD44 antibody Cat. No. 566116/566200; solid line histogram . The fluorescence histogram showing CD44 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable bone marrow cells. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System.