BD HorizonTM BV421 Mouse Anti-Human OX40 Ligand (CD252)

Description

Flow cytometric analysis of OX40 Ligand expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were preincubated with recombinant OX40 Ligand and stimulated with phytohemagglutinin PHA; Sigma L-1668 for 3 days. The cells were then stained with either BD Horizon BV421 Mouse IgG1, k Isotype Control Cat. No. 562438; dashed line histogram or BD Horizon BV421 Mouse Anti-Human OX40 Ligand CD252 Cat. No. 563766; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of OX40 Ligand expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were preincubated with recombinant OX40 Ligand and stimulated with phytohemagglutinin PHA; Sigma L-1668 for 3 days. The cells were then stained with either BD Horizon BV421 Mouse IgG1, k Isotype Control Cat. No. 562438; dashed line histogram or BD Horizon BV421 Mouse Anti-Human OX40 Ligand CD252 Cat. No. 563766; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of OX40 Ligand expression on human peripheral blood lymphocytes. Human peripheral blood mononuclear cells were preincubated with recombinant OX40 Ligand and stimulated with phytohemagglutinin PHA; Sigma L-1668 for 3 days. The cells were then stained with either BD Horizon BV421 Mouse IgG1, k Isotype Control Cat. No. 562438; dashed line histogram or BD Horizon BV421 Mouse Anti-Human OX40 Ligand CD252 Cat. No. 563766; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD LSR II Flow Cytometer System.