BD HorizonTM BV605 Mouse Anti-Human IgD

Description

Two-color flow cytometric analysis of IgD expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were incubated in complete tissue culture medium overnight in order to minimize subsequent nonspecific immunofluorescent staining. The cells were harvested and stained with APC Mouse Anti-Human CD19 antibody Cat. No. 555415/561742 and with either BD Horizon BV605 Mouse IgG2a, kappa Isotype Control Cat. No. 562778; Left Panel or BD Horizon BV605 Mouse Anti-Human IgD antibody Cat. No. 563313; Right Panel . The two-color flow cytometric dot plots showing the correlated expression of IgD or Ig isotype control staining versus CD19 were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Two-color flow cytometric analysis of IgD expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were incubated in complete tissue culture medium overnight in order to minimize subsequent nonspecific immunofluorescent staining. The cells were harvested and stained with APC Mouse Anti-Human CD19 antibody Cat. No. 555415/561742 and with either BD Horizon BV605 Mouse IgG2a, kappa Isotype Control Cat. No. 562778; Left Panel or BD Horizon BV605 Mouse Anti-Human IgD antibody Cat. No. 563313; Right Panel . The two-color flow cytometric dot plots showing the correlated expression of IgD or Ig isotype control staining versus CD19 were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Two-color flow cytometric analysis of IgD expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were incubated in complete tissue culture medium overnight in order to minimize subsequent nonspecific immunofluorescent staining. The cells were harvested and stained with APC Mouse Anti-Human CD19 antibody Cat. No. 555415/561742 and with either BD Horizon BV605 Mouse IgG2a, kappa Isotype Control Cat. No. 562778; Left Panel or BD Horizon BV605 Mouse Anti-Human IgD antibody Cat. No. 563313; Right Panel . The two-color flow cytometric dot plots showing the correlated expression of IgD or Ig isotype control staining versus CD19 were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Two-color flow cytometric analysis of IgD expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were incubated in complete tissue culture medium overnight in order to minimize subsequent nonspecific immunofluorescent staining. The cells were harvested and stained with APC Mouse Anti-Human CD19 antibody Cat. No. 555415/561742 and with either BD Horizon BV605 Mouse IgG2a, kappa Isotype Control Cat. No. 562778; Left Panel or BD Horizon BV605 Mouse Anti-Human IgD antibody Cat. No. 563313; Right Panel . The two-color flow cytometric dot plots showing the correlated expression of IgD or Ig isotype control staining versus CD19 were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Two-color flow cytometric analysis of IgD expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were incubated in complete tissue culture medium overnight in order to minimize subsequent nonspecific immunofluorescent staining. The cells were harvested and stained with APC Mouse Anti-Human CD19 antibody Cat. No. 555415/561742 and with either BD Horizon BV605 Mouse IgG2a, kappa Isotype Control Cat. No. 562778; Left Panel or BD Horizon BV605 Mouse Anti-Human IgD antibody Cat. No. 563313; Right Panel . The two-color flow cytometric dot plots showing the correlated expression of IgD or Ig isotype control staining versus CD19 were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Two-color flow cytometric analysis of IgD expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were incubated in complete tissue culture medium overnight in order to minimize subsequent nonspecific immunofluorescent staining. The cells were harvested and stained with APC Mouse Anti-Human CD19 antibody Cat. No. 555415/561742 and with either BD Horizon BV605 Mouse IgG2a, kappa Isotype Control Cat. No. 562778; Left Panel or BD Horizon BV605 Mouse Anti-Human IgD antibody Cat. No. 563313; Right Panel . The two-color flow cytometric dot plots showing the correlated expression of IgD or Ig isotype control staining versus CD19 were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System.