BD HorizonTM BUV661 Rat Anti-Mouse CD45R/B220

Description

Two-color flow cytometric analysis of B220/CD45R expression on mouse splenocytes. Mouse splenic leucocytes were stained with Alexa Fluor 488 Hamster Anti-Mouse CD3e antibody Cat. No. 557666 and either BD Horizon BUV661 Rat IgG2a, kappa Isotype Control Cat. No. 565075; Left Panel or BD Horizon BUV661 Rat Anti-Mouse B220/CD45R antibody Cat. No. 565077; Right Panel . The two-color flow cytometric contour plot showing the correlated expression of B220/CD45R or Ig Isotype control staining versus CD3e was derived from gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Two-color flow cytometric analysis of B220/CD45R expression on mouse splenocytes. Mouse splenic leucocytes were stained with Alexa Fluor 488 Hamster Anti-Mouse CD3e antibody Cat. No. 557666 and either BD Horizon BUV661 Rat IgG2a, kappa Isotype Control Cat. No. 565075; Left Panel or BD Horizon BUV661 Rat Anti-Mouse B220/CD45R antibody Cat. No. 565077; Right Panel . The two-color flow cytometric contour plot showing the correlated expression of B220/CD45R or Ig Isotype control staining versus CD3e was derived from gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Two-color flow cytometric analysis of B220/CD45R expression on mouse splenocytes. Mouse splenic leucocytes were stained with Alexa Fluor 488 Hamster Anti-Mouse CD3e antibody Cat. No. 557666 and either BD Horizon BUV661 Rat IgG2a, kappa Isotype Control Cat. No. 565075; Left Panel or BD Horizon BUV661 Rat Anti-Mouse B220/CD45R antibody Cat. No. 565077; Right Panel . The two-color flow cytometric contour plot showing the correlated expression of B220/CD45R or Ig Isotype control staining versus CD3e was derived from gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Show More Two-color flow cytometric analysis of B220/CD45R expression on mouse splenocytes. Mouse splenic leucocytes were stained with Alexa Fluor 488 Hamster Anti-Mouse CD3e antibody Cat. No. 557666 and either BD Horizon BUV661 Rat IgG2a, kappa Isotype Control Cat. No. 565075; Left Panel or BD Horizon BUV661 Rat Anti-Mouse B220/CD45R antibody Cat. No. 565077; Right Panel . The two-color flow cytometric contour plot showing the correlated expression of B220/CD45R or Ig Isotype control staining versus CD3e was derived from gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Show More Two-color flow cytometric analysis of B220/CD45R expression on mouse splenocytes. Mouse splenic leucocytes were stained with Alexa Fluor 488 Hamster Anti-Mouse CD3e antibody Cat. No. 557666 and either BD Horizon BUV661 Rat IgG2a, kappa Isotype Control Cat. No. 565075; Left Panel or BD Horizon BUV661 Rat Anti-Mouse B220/CD45R antibody Cat. No. 565077; Right Panel . The two-color flow cytometric contour plot showing the correlated expression of B220/CD45R or Ig Isotype control staining versus CD3e was derived from gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Two-color flow cytometric analysis of B220/CD45R expression on mouse splenocytes. Mouse splenic leucocytes were stained with Alexa Fluor 488 Hamster Anti-Mouse CD3e antibody Cat. No. 557666 and either BD Horizon BUV661 Rat IgG2a, kappa Isotype Control Cat. No. 565075; Left Panel or BD Horizon BUV661 Rat Anti-Mouse B220/CD45R antibody Cat. No. 565077; Right Panel . The two-color flow cytometric contour plot showing the correlated expression of B220/CD45R or Ig Isotype control staining versus CD3e was derived from gated events with the forward and side light-scatter characteristics of viable splenic leucocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System.