BD HorizonTM BUV395 Mouse Anti-Human CD278

Description

Flow cytometric analysis of CD278 expression on stimulated human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were cultured with Phytohemagglutinin PHA; Sigma L-1668 for 3 days. The stimulated cells were then stained with either BD Horizon BUV395 Mouse IgG1 kappa Isotype Control Cat. No. 563547; dashed line histogram or BD Horizon BUV395 Mouse Anti-Human CD278 antibody Cat. No. 564777; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphoblasts. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Flow cytometric analysis of CD278 expression on stimulated human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were cultured with Phytohemagglutinin PHA; Sigma L-1668 for 3 days. The stimulated cells were then stained with either BD Horizon BUV395 Mouse IgG1 kappa Isotype Control Cat. No. 563547; dashed line histogram or BD Horizon BUV395 Mouse Anti-Human CD278 antibody Cat. No. 564777; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphoblasts. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Show More Flow cytometric analysis of CD278 expression on stimulated human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were cultured with Phytohemagglutinin PHA; Sigma L-1668 for 3 days. The stimulated cells were then stained with either BD Horizon BUV395 Mouse IgG1 kappa Isotype Control Cat. No. 563547; dashed line histogram or BD Horizon BUV395 Mouse Anti-Human CD278 antibody Cat. No. 564777; solid line histogram . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphoblasts. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System.