BD PharmingenTM PE Rat Anti-Human CD49f

Description

Flow cytometric analysis of CD49f expression on human peripheral blood lymphocytes. Human whole blood was stained with either PE Rat IgG2a, kappa Isotype Control Cat. No. 555844; dashed line histogram or PE Rat Anti-Human CD49f Cat. No. 555736/561894; solid line histogram . Erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Fluorescent histograms depicting CD49f or Ig isotype expression were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD FACScan system. Flow cytometric analysis of CD49f expression on human peripheral blood lymphocytes. Human whole blood was stained with either PE Rat IgG2a, kappa Isotype Control Cat. No. 555844; dashed line histogram or PE Rat Anti-Human CD49f Cat. No. 555736/561894; solid line histogram . Erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Fluorescent histograms depicting CD49f or Ig isotype expression were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD FACScan system. Show More Flow cytometric analysis of CD49f expression on human peripheral blood lymphocytes. Human whole blood was stained with either PE Rat IgG2a, kappa Isotype Control Cat. No. 555844; dashed line histogram or PE Rat Anti-Human CD49f Cat. No. 555736/561894; solid line histogram . Erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Fluorescent histograms depicting CD49f or Ig isotype expression were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD FACScan system.