
563360 ·
BDB Bioscience · Cat: 563360
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bdbiosciences.com/en-us/products/reagents/flow-cytometry-rea...Description
Flow cytometric analysis of CD62E expression on HUVEC cells. Human Umbilical Vein Endothelial Cells HUVEC were either untreated Left Panel or cultured with Recombinant Human TNF protein Cat. No. 554618; 20 ng/ml; Right Panel for 4 hours at 37C. The cells were stained with BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; dashed line histogram or BD Horizon BV421 Mouse Anti-Human CD62E antibody Cat. No. 563360; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Flow cytometric analysis of CD62E expression on HUVEC cells. Human Umbilical Vein Endothelial Cells HUVEC were either untreated Left Panel or cultured with Recombinant Human TNF protein Cat. No. 554618; 20 ng/ml; Right Panel for 4 hours at 37C. The cells were stained with BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; dashed line histogram or BD Horizon BV421 Mouse Anti-Human CD62E antibody Cat. No. 563360; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Flow cytometric analysis of CD62E expression on HUVEC cells. Human Umbilical Vein Endothelial Cells HUVEC were either untreated Left Panel or cultured with Recombinant Human TNF protein Cat. No. 554618; 20 ng/ml; Right Panel for 4 hours at 37C. The cells were stained with BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; dashed line histogram or BD Horizon BV421 Mouse Anti-Human CD62E antibody Cat. No. 563360; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Show More Flow cytometric analysis of CD62E expression on HUVEC cells. Human Umbilical Vein Endothelial Cells HUVEC were either untreated Left Panel or cultured with Recombinant Human TNF protein Cat. No. 554618; 20 ng/ml; Right Panel for 4 hours at 37C. The cells were stained with BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; dashed line histogram or BD Horizon BV421 Mouse Anti-Human CD62E antibody Cat. No. 563360; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Show More Flow cytometric analysis of CD62E expression on HUVEC cells. Human Umbilical Vein Endothelial Cells HUVEC were either untreated Left Panel or cultured with Recombinant Human TNF protein Cat. No. 554618; 20 ng/ml; Right Panel for 4 hours at 37C. The cells were stained with BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; dashed line histogram or BD Horizon BV421 Mouse Anti-Human CD62E antibody Cat. No. 563360; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System. Flow cytometric analysis of CD62E expression on HUVEC cells. Human Umbilical Vein Endothelial Cells HUVEC were either untreated Left Panel or cultured with Recombinant Human TNF protein Cat. No. 554618; 20 ng/ml; Right Panel for 4 hours at 37C. The cells were stained with BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; dashed line histogram or BD Horizon BV421 Mouse Anti-Human CD62E antibody Cat. No. 563360; solid line histogram . The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable cells. Flow cytometric analysis was performed using a BD LSRFortessa Cell Analyzer System.