



























参考图片
Flow cytometric analysis of HLA-DR expression on human peripheral blood lymphocytes and monocytes. Human whole blood was stained with the BD Horizon™ BV510 Mouse Anti-Human HLA-DR antibody (Cat. No. 563083; solid line histogram) or with a BD Horizon™ BV510 Mouse IgG2a, κ Isotype Control (Cat. No. 563027; dashed line histogram). The erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes (Left Panel) or monocytes (Right Panel). Flow cytometric analysis was performed using a BD LSRFortessa™ Cell Analyzer System.
Flow cytometric analysis of HLA-DR expression on human peripheral blood lymphocytes and monocytes. Human whole blood was stained with the BD Horizon™ BV510 Mouse Anti-Human HLA-DR antibody (Cat. No. 563083; solid line histogram) or with a BD Horizon™ BV510 Mouse IgG2a, κ Isotype Control (Cat. No. 563027; dashed line histogram). The erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes (Left Panel) or monocytes (Right Panel). Flow cytometric analysis was performed using a BD LSRFortessa™ Cell Analyzer System.