BD PharmingenTM PE Mouse Anti-Human PD-L1 (CD274)

Description

Flow cytometric analysis of human PD-L1 CD274 expression on activated human lymphocytes. Human peripheral blood mononuclear cells were stimulated with Phytohemagglutinin PHA for 3 days and were stained with either Mouse IgG2b, kappa Isotype Control Cat. No. 555058; dotted line histogram or PE Mouse Anti-Human PD-L1 CD274 antibody Cat. No. 568079/568080; solid line histogram . The fluorescence histogram showing the expression of CD274 or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of activated viable lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System and FlowJo software. Data shown on this Technical Data Sheet are not lot specific. Flow cytometric analysis of human PD-L1 CD274 expression on activated human lymphocytes. Human peripheral blood mononuclear cells were stimulated with Phytohemagglutinin PHA for 3 days and were stained with either Mouse IgG2b, kappa Isotype Control Cat. No. 555058; dotted line histogram or PE Mouse Anti-Human PD-L1 CD274 antibody Cat. No. 568079/568080; solid line histogram . The fluorescence histogram showing the expression of CD274 or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of activated viable lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System and FlowJo software. Data shown on this Technical Data Sheet are not lot specific. Show More Flow cytometric analysis of human PD-L1 CD274 expression on activated human lymphocytes. Human peripheral blood mononuclear cells were stimulated with Phytohemagglutinin PHA for 3 days and were stained with either Mouse IgG2b, kappa Isotype Control Cat. No. 555058; dotted line histogram or PE Mouse Anti-Human PD-L1 CD274 antibody Cat. No. 568079/568080; solid line histogram . The fluorescence histogram showing the expression of CD274 or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of activated viable lymphocytes. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System and FlowJo software. Data shown on this Technical Data Sheet are not lot specific.