BD HorizonTM BV711 Mouse Anti-Human CD24

Description

Flow cytometric analysis of CD24 expression on human peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD19 antibody 555415/561742 and either BD Horizon BV711 Mouse IgG2a, kappa Isotype Control Cat. No. 563345; Left Panel or BD Horizon BV711 Mouse Anti-Human CD24 antibody Cat. No. 563401/563371; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-color flow cytometric dot plots show the correlated expression patterns of CD24 versus CD19 for gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD24 expression on human peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD19 antibody 555415/561742 and either BD Horizon BV711 Mouse IgG2a, kappa Isotype Control Cat. No. 563345; Left Panel or BD Horizon BV711 Mouse Anti-Human CD24 antibody Cat. No. 563401/563371; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-color flow cytometric dot plots show the correlated expression patterns of CD24 versus CD19 for gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD24 expression on human peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD19 antibody 555415/561742 and either BD Horizon BV711 Mouse IgG2a, kappa Isotype Control Cat. No. 563345; Left Panel or BD Horizon BV711 Mouse Anti-Human CD24 antibody Cat. No. 563401/563371; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-color flow cytometric dot plots show the correlated expression patterns of CD24 versus CD19 for gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD24 expression on human peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD19 antibody 555415/561742 and either BD Horizon BV711 Mouse IgG2a, kappa Isotype Control Cat. No. 563345; Left Panel or BD Horizon BV711 Mouse Anti-Human CD24 antibody Cat. No. 563401/563371; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-color flow cytometric dot plots show the correlated expression patterns of CD24 versus CD19 for gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD24 expression on human peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD19 antibody 555415/561742 and either BD Horizon BV711 Mouse IgG2a, kappa Isotype Control Cat. No. 563345; Left Panel or BD Horizon BV711 Mouse Anti-Human CD24 antibody Cat. No. 563401/563371; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-color flow cytometric dot plots show the correlated expression patterns of CD24 versus CD19 for gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD24 expression on human peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD19 antibody 555415/561742 and either BD Horizon BV711 Mouse IgG2a, kappa Isotype Control Cat. No. 563345; Left Panel or BD Horizon BV711 Mouse Anti-Human CD24 antibody Cat. No. 563401/563371; Right Panel . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The two-color flow cytometric dot plots show the correlated expression patterns of CD24 versus CD19 for gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System.