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Flow cytometric analysis of CD25 expression on unstimulated and stimulated mouse splenocytes. Left and Middle Panels: Freshly prepared 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 either BD Horizon™ BB515 Rat IgG1, λ Isotype Control (Cat. No. 564417; Left Panel) or BD Horizon™ BB515 Rat Anti-Mouse CD25 antibody (Cat. No. 564424/564458; Middle Panel). Two-color flow cytometric contour plots showing the correlated expression patterns for Ig Isotype control staining (Left Panel) or CD25 expression (Middle Panel) versus cellular autofluorescence (measured in the APC/allophycocyanin channel) were generated for gated events with the forward and side light- scatter characteristics of viable lymphocytes. Right Panel: Mouse splenic leucocytes were stimulated with concanavalin A for 3 days. The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™). The cells were then stained with either BD Horizon™ BB515 Rat IgG1, λ Isotype Control (dashed line histogram) or BD Horizon™ BB515 Rat Anti-Mouse CD25 antibody (solid line histogram). The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable lymphoblasts. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of CD25 expression on unstimulated and stimulated mouse splenocytes. Left and Middle Panels: Freshly prepared 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 either BD Horizon™ BB515 Rat IgG1, λ Isotype Control (Cat. No. 564417; Left Panel) or BD Horizon™ BB515 Rat Anti-Mouse CD25 antibody (Cat. No. 564424/564458; Middle Panel). Two-color flow cytometric contour plots showing the correlated expression patterns for Ig Isotype control staining (Left Panel) or CD25 expression (Middle Panel) versus cellular autofluorescence (measured in the APC/allophycocyanin channel) were generated for gated events with the forward and side light- scatter characteristics of viable lymphocytes. Right Panel: Mouse splenic leucocytes were stimulated with concanavalin A for 3 days. The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody (Mouse BD Fc Block™). The cells were then stained with either BD Horizon™ BB515 Rat IgG1, λ Isotype Control (dashed line histogram) or BD Horizon™ BB515 Rat Anti-Mouse CD25 antibody (solid line histogram). The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable lymphoblasts. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.