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 FITC Anti-Mouse IgM[a] antibody (Cat. No. 553516) and either PE Rat IgG2a, κ Isotype Control ( Cat. No. 553930; Left Panel) or PE Rat Anti-Mouse CD23 antibody (Cat. No. 561773/553139; 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 FITC Anti-Mouse IgM[a] antibody (Cat. No. 553516) and either PE Rat IgG2a, κ Isotype Control ( Cat. No. 553930; Left Panel) or PE Rat Anti-Mouse CD23 antibody (Cat. No. 561773/553139; 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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