BD HorizonTM APC-R700 Mouse Anti-Human CD196 (CCR6)

Description

Flow cytometric analysis of CD196 CCR6 expression on human peripheral blood lymphocytes. Human whole blood was stained with either BD Horizon APC-R700 Mouse IgG1, kappa Isotype Control Cat. No. 564974; dashed line histogram or BD Horizon APC-R700 Mouse Anti-Human CD196 CCR6 antibody Cat. No. 565173; solid line histogram . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The fluorescence histogram showing CD196 CCR6 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD196 CCR6 expression on human peripheral blood lymphocytes. Human whole blood was stained with either BD Horizon APC-R700 Mouse IgG1, kappa Isotype Control Cat. No. 564974; dashed line histogram or BD Horizon APC-R700 Mouse Anti-Human CD196 CCR6 antibody Cat. No. 565173; solid line histogram . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The fluorescence histogram showing CD196 CCR6 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD196 CCR6 expression on human peripheral blood lymphocytes. Human whole blood was stained with either BD Horizon APC-R700 Mouse IgG1, kappa Isotype Control Cat. No. 564974; dashed line histogram or BD Horizon APC-R700 Mouse Anti-Human CD196 CCR6 antibody Cat. No. 565173; solid line histogram . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . The fluorescence histogram showing CD196 CCR6 expression or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System.