
564023 ·
BDB Bioscience · Cat: 564023
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Description
Flow cytometric analysis of CD25 expression on unstimulated and stimulated mouse splenocytes. Left and Middle Panels: 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 Rat Anti-Mouse CD4 antibody Cat. No. 553047/553046/561835 and either BD Horizon BV786 Rat IgG1, lambda Isotype Control Cat. No. 564093; Left Panel or BD Horizon BV786 Rat Anti-Mouse CD25 antibody Cat. No. 564023; Middle Panel . Two-color flow cytometric dot plots show the correlated expression patterns for CD25 or Ig Isotype control staining versus CD4 for events with the forward and side light-scatter characteristics of viable splenocytes. Right Panel: Mouse splenic leucocytes were stimulated for 3 days with concanavalin A. The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody and then stained with either BD Horizon BV786 Rat IgG1, lambda Isotype Control dashed line histogram or BD Horizon BV786 Rat Anti-Mouse CD25 antibody solid line histogram . The fluorescence histograms were derived from 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: 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 Rat Anti-Mouse CD4 antibody Cat. No. 553047/553046/561835 and either BD Horizon BV786 Rat IgG1, lambda Isotype Control Cat. No. 564093; Left Panel or BD Horizon BV786 Rat Anti-Mouse CD25 antibody Cat. No. 564023; Middle Panel . Two-color flow cytometric dot plots show the correlated expression patterns for CD25 or Ig Isotype control staining versus CD4 for events with the forward and side light-scatter characteristics of viable splenocytes. Right Panel: Mouse splenic leucocytes were stimulated for 3 days with concanavalin A. The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody and then stained with either BD Horizon BV786 Rat IgG1, lambda Isotype Control dashed line histogram or BD Horizon BV786 Rat Anti-Mouse CD25 antibody solid line histogram . The fluorescence histograms were derived from 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: 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 Rat Anti-Mouse CD4 antibody Cat. No. 553047/553046/561835 and either BD Horizon BV786 Rat IgG1, lambda Isotype Control Cat. No. 564093; Left Panel or BD Horizon BV786 Rat Anti-Mouse CD25 antibody Cat. No. 564023; Middle Panel . Two-color flow cytometric dot plots show the correlated expression patterns for CD25 or Ig Isotype control staining versus CD4 for events with the forward and side light-scatter characteristics of viable splenocytes. Right Panel: Mouse splenic leucocytes were stimulated for 3 days with concanavalin A. The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody and then stained with either BD Horizon BV786 Rat IgG1, lambda Isotype Control dashed line histogram or BD Horizon BV786 Rat Anti-Mouse CD25 antibody solid line histogram . The fluorescence histograms were derived from 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. Show More Flow cytometric analysis of CD25 expression on unstimulated and stimulated mouse splenocytes. Left and Middle Panels: 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 Rat Anti-Mouse CD4 antibody Cat. No. 553047/553046/561835 and either BD Horizon BV786 Rat IgG1, lambda Isotype Control Cat. No. 564093; Left Panel or BD Horizon BV786 Rat Anti-Mouse CD25 antibody Cat. No. 564023; Middle Panel . Two-color flow cytometric dot plots show the correlated expression patterns for CD25 or Ig Isotype control staining versus CD4 for events with the forward and side light-scatter characteristics of viable splenocytes. Right Panel: Mouse splenic leucocytes were stimulated for 3 days with concanavalin A. The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody and then stained with either BD Horizon BV786 Rat IgG1, lambda Isotype Control dashed line histogram or BD Horizon BV786 Rat Anti-Mouse CD25 antibody solid line histogram . The fluorescence histograms were derived from 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. Show More Flow cytometric analysis of CD25 expression on unstimulated and stimulated mouse splenocytes. Left and Middle Panels: 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 Rat Anti-Mouse CD4 antibody Cat. No. 553047/553046/561835 and either BD Horizon BV786 Rat IgG1, lambda Isotype Control Cat. No. 564093; Left Panel or BD Horizon BV786 Rat Anti-Mouse CD25 antibody Cat. No. 564023; Middle Panel . Two-color flow cytometric dot plots show the correlated expression patterns for CD25 or Ig Isotype control staining versus CD4 for events with the forward and side light-scatter characteristics of viable splenocytes. Right Panel: Mouse splenic leucocytes were stimulated for 3 days with concanavalin A. The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody and then stained with either BD Horizon BV786 Rat IgG1, lambda Isotype Control dashed line histogram or BD Horizon BV786 Rat Anti-Mouse CD25 antibody solid line histogram . The fluorescence histograms were derived from 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: 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 Rat Anti-Mouse CD4 antibody Cat. No. 553047/553046/561835 and either BD Horizon BV786 Rat IgG1, lambda Isotype Control Cat. No. 564093; Left Panel or BD Horizon BV786 Rat Anti-Mouse CD25 antibody Cat. No. 564023; Middle Panel . Two-color flow cytometric dot plots show the correlated expression patterns for CD25 or Ig Isotype control staining versus CD4 for events with the forward and side light-scatter characteristics of viable splenocytes. Right Panel: Mouse splenic leucocytes were stimulated for 3 days with concanavalin A. The cells were preincubated with Purified Rat Anti-Mouse CD16/CD32 antibody and then stained with either BD Horizon BV786 Rat IgG1, lambda Isotype Control dashed line histogram or BD Horizon BV786 Rat Anti-Mouse CD25 antibody solid line histogram . The fluorescence histograms were derived from 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.