BD HorizonTM BUV395 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 BD Horizon BUV395 Mouse IgG2b, kappa Isotype Control Cat. No. 563558; dotted line histogram or BD Horizon BUV395 Mouse Anti-Human PD-L1 CD274 antibody Cat. No. 568620/568621; solid line histogram . The fluorescence histogram showing the expression of PD-L1 CD274 or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of activated viable lymphocytes. Flow cytometriy 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 BD Horizon BUV395 Mouse IgG2b, kappa Isotype Control Cat. No. 563558; dotted line histogram or BD Horizon BUV395 Mouse Anti-Human PD-L1 CD274 antibody Cat. No. 568620/568621; solid line histogram . The fluorescence histogram showing the expression of PD-L1 CD274 or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of activated viable lymphocytes. Flow cytometriy 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 BD Horizon BUV395 Mouse IgG2b, kappa Isotype Control Cat. No. 563558; dotted line histogram or BD Horizon BUV395 Mouse Anti-Human PD-L1 CD274 antibody Cat. No. 568620/568621; solid line histogram . The fluorescence histogram showing the expression of PD-L1 CD274 or Ig Isotype control staining was derived from gated events with the forward and side light-scatter characteristics of activated viable lymphocytes. Flow cytometriy and data analysis were performed using a BD LSRFortessa X-20 Cell Analyzer System and FlowJo software.