BD PharmingenTM Purified NA/LE Mouse Anti-Human CD3

Description

Flow cytometric analysis of CD3 expression on human peripheral blood lymphocytes. Human whole blood was stained with either Purified NA/LE Mouse IgG1 kappa Isotype Control Cat. No. 554721; dashed line histogram or Purified NA/LE Mouse Anti-Human CD3 antibody Cat. No. 555329/562280/562310; solid line histogram . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The cells were washed and then stained with FITC Goat Anti-Mouse IgG/IgM Cat. No. 562292; dashed line histogram . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms 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 CD3 expression on human peripheral blood lymphocytes. Human whole blood was stained with either Purified NA/LE Mouse IgG1 kappa Isotype Control Cat. No. 554721; dashed line histogram or Purified NA/LE Mouse Anti-Human CD3 antibody Cat. No. 555329/562280/562310; solid line histogram . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The cells were washed and then stained with FITC Goat Anti-Mouse IgG/IgM Cat. No. 562292; dashed line histogram . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms 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 CD3 expression on human peripheral blood lymphocytes. Human whole blood was stained with either Purified NA/LE Mouse IgG1 kappa Isotype Control Cat. No. 554721; dashed line histogram or Purified NA/LE Mouse Anti-Human CD3 antibody Cat. No. 555329/562280/562310; solid line histogram . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The cells were washed and then stained with FITC Goat Anti-Mouse IgG/IgM Cat. No. 562292; dashed line histogram . The erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms 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.