BD PharmingenTM APC Mouse anti-Human Ig, kappa Light Chain

Description

Flow cytometric analysis of Ig kappa Light Chain expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells PBMC 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 Cat. No. 557697 and either APC Mouse anti-Human Ig kappa Light Chain antibody Cat. No. 561323; Right Panel or APC Mouse IgG1, kappa Isotype Control Cat. No. 554681; Left Panel and. The two-color flow cytometric dot plots showing the correlated expression of Ig kappa Light Chain 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 Ig kappa Light Chain expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells PBMC 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 Cat. No. 557697 and either APC Mouse anti-Human Ig kappa Light Chain antibody Cat. No. 561323; Right Panel or APC Mouse IgG1, kappa Isotype Control Cat. No. 554681; Left Panel and. The two-color flow cytometric dot plots showing the correlated expression of Ig kappa Light Chain 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 Ig kappa Light Chain expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells PBMC 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 Cat. No. 557697 and either APC Mouse anti-Human Ig kappa Light Chain antibody Cat. No. 561323; Right Panel or APC Mouse IgG1, kappa Isotype Control Cat. No. 554681; Left Panel and. The two-color flow cytometric dot plots showing the correlated expression of Ig kappa Light Chain 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 Ig kappa Light Chain expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells PBMC 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 Cat. No. 557697 and either APC Mouse anti-Human Ig kappa Light Chain antibody Cat. No. 561323; Right Panel or APC Mouse IgG1, kappa Isotype Control Cat. No. 554681; Left Panel and. The two-color flow cytometric dot plots showing the correlated expression of Ig kappa Light Chain 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 Ig kappa Light Chain expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells PBMC 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 Cat. No. 557697 and either APC Mouse anti-Human Ig kappa Light Chain antibody Cat. No. 561323; Right Panel or APC Mouse IgG1, kappa Isotype Control Cat. No. 554681; Left Panel and. The two-color flow cytometric dot plots showing the correlated expression of Ig kappa Light Chain 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 Ig kappa Light Chain expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells PBMC 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 Cat. No. 557697 and either APC Mouse anti-Human Ig kappa Light Chain antibody Cat. No. 561323; Right Panel or APC Mouse IgG1, kappa Isotype Control Cat. No. 554681; Left Panel and. The two-color flow cytometric dot plots showing the correlated expression of Ig kappa Light Chain 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.