参考图片
Two-color flow cytometric analysis of CD23 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 Anti-Mouse IgM[a] antibody (Cat. No. 553517) and either FITC Rat IgG2a, κ Isotype Control ( Cat. No. 553929; Left Panel) or FITC Rat Anti-Mouse CD23 antibody (Cat. No. 561772/553138; Right Panel). Two-color flow cytometric dot plots show the correlated expression patterns of CD23 (or Ig Isotype control staining) versus IgM for gated events with the forward and side light-scatter characteristics of viable splenic leucocytes.
Two-color flow cytometric analysis of CD23 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 Anti-Mouse IgM[a] antibody (Cat. No. 553517) and either FITC Rat IgG2a, κ Isotype Control ( Cat. No. 553929; Left Panel) or FITC Rat Anti-Mouse CD23 antibody (Cat. No. 561772/553138; Right Panel). Two-color flow cytometric dot plots show the correlated expression patterns of CD23 (or Ig Isotype control staining) versus IgM for gated events with the forward and side light-scatter characteristics of viable splenic leucocytes.
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