BD PharmingenTM Alexa Fluor 700 Mouse Anti-Human IgD

Description

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 Alexa Fluor 488 Mouse anti-Human CD19 antibody Cat. No. 557697 and with either an Alexa Fluor 700 Mouse IgG2a, kappa Isotype Control Cat. No. 557880; Left Panel or an Alexa Fluor 700 Mouse anti-Human IgD antibody Cat. No. 561302; 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 cytometry was performed using a BD LSR II Flow Cytometer System. 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 Alexa Fluor 488 Mouse anti-Human CD19 antibody Cat. No. 557697 and with either an Alexa Fluor 700 Mouse IgG2a, kappa Isotype Control Cat. No. 557880; Left Panel or an Alexa Fluor 700 Mouse anti-Human IgD antibody Cat. No. 561302; 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 cytometry was performed using a BD LSR II Flow Cytometer System. 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 Alexa Fluor 488 Mouse anti-Human CD19 antibody Cat. No. 557697 and with either an Alexa Fluor 700 Mouse IgG2a, kappa Isotype Control Cat. No. 557880; Left Panel or an Alexa Fluor 700 Mouse anti-Human IgD antibody Cat. No. 561302; 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 cytometry was performed using a BD LSR II Flow Cytometer System. Show More 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 Alexa Fluor 488 Mouse anti-Human CD19 antibody Cat. No. 557697 and with either an Alexa Fluor 700 Mouse IgG2a, kappa Isotype Control Cat. No. 557880; Left Panel or an Alexa Fluor 700 Mouse anti-Human IgD antibody Cat. No. 561302; 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 cytometry was performed using a BD LSR II Flow Cytometer System. Show More 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 Alexa Fluor 488 Mouse anti-Human CD19 antibody Cat. No. 557697 and with either an Alexa Fluor 700 Mouse IgG2a, kappa Isotype Control Cat. No. 557880; Left Panel or an Alexa Fluor 700 Mouse anti-Human IgD antibody Cat. No. 561302; 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 cytometry was performed using a BD LSR II Flow Cytometer System. 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 Alexa Fluor 488 Mouse anti-Human CD19 antibody Cat. No. 557697 and with either an Alexa Fluor 700 Mouse IgG2a, kappa Isotype Control Cat. No. 557880; Left Panel or an Alexa Fluor 700 Mouse anti-Human IgD antibody Cat. No. 561302; 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 cytometry was performed using a BD LSR II Flow Cytometer System.