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

Description

Flow cytometric analysis of PD-L1 CD274 expression on activated human lymphocytes. Human peripheral blood mononuclear cells were stimulated with Phytohemagglutinin PHA for 3 days and stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dotted line histogram or PE Mouse Anti-Human PD-L1 CD274 antibody Cat. No. 568721/568722; solid line histogram . The fluorescence histogram showing the expression of PD-L1 CD274 or Ig Isotype control staining was derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Flow cytometric analysis of PD-L1 CD274 expression on activated human lymphocytes. Human peripheral blood mononuclear cells were stimulated with Phytohemagglutinin PHA for 3 days and stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dotted line histogram or PE Mouse Anti-Human PD-L1 CD274 antibody Cat. No. 568721/568722; solid line histogram . The fluorescence histogram showing the expression of PD-L1 CD274 or Ig Isotype control staining was derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software. Show More Flow cytometric analysis of PD-L1 CD274 expression on activated human lymphocytes. Human peripheral blood mononuclear cells were stimulated with Phytohemagglutinin PHA for 3 days and stained with either PE Mouse IgG1, kappa Isotype Control Cat. No. 554680; dotted line histogram or PE Mouse Anti-Human PD-L1 CD274 antibody Cat. No. 568721/568722; solid line histogram . The fluorescence histogram showing the expression of PD-L1 CD274 or Ig Isotype control staining was derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software.