BD PharmingenTM PE Mouse anti-Human CD52

Description

Flow cytometric analysis of human CD52 expression on human peripheral blood lymphocytes. Whole blood was treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to remove erythrocytes. The cells were washed and then stained with either PE Mouse IgG3, kappa Isotype Control Cat. No. 556659; dashed line histogram or PE Mouse Anti-Human CD52 Cat. No. 562945; solid line histogram . The fluorescence histograms were derived from 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 human CD52 expression on human peripheral blood lymphocytes. Whole blood was treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to remove erythrocytes. The cells were washed and then stained with either PE Mouse IgG3, kappa Isotype Control Cat. No. 556659; dashed line histogram or PE Mouse Anti-Human CD52 Cat. No. 562945; solid line histogram . The fluorescence histograms were derived from 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 human CD52 expression on human peripheral blood lymphocytes. Whole blood was treated with BD Pharm Lyse Lysing Buffer Cat. No. 555899 to remove erythrocytes. The cells were washed and then stained with either PE Mouse IgG3, kappa Isotype Control Cat. No. 556659; dashed line histogram or PE Mouse Anti-Human CD52 Cat. No. 562945; solid line histogram . The fluorescence histograms were derived from 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.