BD HorizonTM BV480 Rat Anti-CD11b

Description

Flow cytometric analysis of CD11b expression on mouse bone-marrow cells. 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-CD11b antibody Cat. No. 566117/566149; solid line histogram . The fluorescence histogram showing CD11b expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of myeloid cells ie, moderate-to-high side light-scatter-gated events . Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Flow cytometric analysis of CD11b expression on mouse bone-marrow cells. 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-CD11b antibody Cat. No. 566117/566149; solid line histogram . The fluorescence histogram showing CD11b expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of myeloid cells ie, moderate-to-high side light-scatter-gated events . Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Show More Flow cytometric analysis of CD11b expression on mouse bone-marrow cells. 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-CD11b antibody Cat. No. 566117/566149; solid line histogram . The fluorescence histogram showing CD11b expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of myeloid cells ie, moderate-to-high side light-scatter-gated events . Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System.