BD PharmingenTM Alexa Fluor 647 Rat Anti-Human CD49f

Description

Flow cytometric analysis of CD49f expression on human peripheral blood lymphocytes. Whole blood was stained with Alexa Fluor 647 Mouse Anti-Human CD49f antibody Cat. No. 562473/562494; solid line histogram or with an Alexa Fluor 647 Rat IgG2a, kappa Isotype Control Cat. No. 557690, 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 CD49f expression on human peripheral blood lymphocytes. Whole blood was stained with Alexa Fluor 647 Mouse Anti-Human CD49f antibody Cat. No. 562473/562494; solid line histogram or with an Alexa Fluor 647 Rat IgG2a, kappa Isotype Control Cat. No. 557690, 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 CD49f expression on human peripheral blood lymphocytes. Whole blood was stained with Alexa Fluor 647 Mouse Anti-Human CD49f antibody Cat. No. 562473/562494; solid line histogram or with an Alexa Fluor 647 Rat IgG2a, kappa Isotype Control Cat. No. 557690, 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.