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Two-color flow cytometric analysis of CD127 expression on mouse splenocytes. 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 PE Hamster Anti-Mouse CD3e antibody (Cat. No. 553064/553063/561824) and either APC Rat IgG2b, κ Isotype Control (Cat. No. 553991; Left Panel) or APC Rat Anti-Mouse CD127 antibody (Cat. No. 564175; Right Panel). Two-color flow cytometric dot plots showing the correlated expression patterns of CD127 (or Ig Isotype control staining) versus CD3e were derived from gated events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.
Two-color flow cytometric analysis of CD127 expression on mouse splenocytes. 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 PE Hamster Anti-Mouse CD3e antibody (Cat. No. 553064/553063/561824) and either APC Rat IgG2b, κ Isotype Control (Cat. No. 553991; Left Panel) or APC Rat Anti-Mouse CD127 antibody (Cat. No. 564175; Right Panel). Two-color flow cytometric dot plots showing the correlated expression patterns of CD127 (or Ig Isotype control staining) versus CD3e were derived from gated events with the forward and side light-scatter characteristics of viable leucocytes. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.