BD PharmingenTM Alexa Fluor 700 Mouse Anti-Human HLA-A2

Description

Flow cytometric analysis of human HLA-A2 on lymphocytes from HLA-A2-positive and -negative donors. Human whole blood from either an HLA-A2-positive Left Panel or an HLA-A2-negative Right Panel donor was stained with the Alexa Fluor 700 Mouse anti-Human HLA-A2 antibody Cat. No. 561339; solid line histogram or with a Alexa Fluor 700 Mouse IgG2b, kappa Isotype Control Cat. No. 560543; dashed line histogram . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of human HLA-A2 on lymphocytes from HLA-A2-positive and -negative donors. Human whole blood from either an HLA-A2-positive Left Panel or an HLA-A2-negative Right Panel donor was stained with the Alexa Fluor 700 Mouse anti-Human HLA-A2 antibody Cat. No. 561339; solid line histogram or with a Alexa Fluor 700 Mouse IgG2b, kappa Isotype Control Cat. No. 560543; dashed line histogram . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of human HLA-A2 on lymphocytes from HLA-A2-positive and -negative donors. Human whole blood from either an HLA-A2-positive Left Panel or an HLA-A2-negative Right Panel donor was stained with the Alexa Fluor 700 Mouse anti-Human HLA-A2 antibody Cat. No. 561339; solid line histogram or with a Alexa Fluor 700 Mouse IgG2b, kappa Isotype Control Cat. No. 560543; dashed line histogram . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of human HLA-A2 on lymphocytes from HLA-A2-positive and -negative donors. Human whole blood from either an HLA-A2-positive Left Panel or an HLA-A2-negative Right Panel donor was stained with the Alexa Fluor 700 Mouse anti-Human HLA-A2 antibody Cat. No. 561339; solid line histogram or with a Alexa Fluor 700 Mouse IgG2b, kappa Isotype Control Cat. No. 560543; dashed line histogram . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of human HLA-A2 on lymphocytes from HLA-A2-positive and -negative donors. Human whole blood from either an HLA-A2-positive Left Panel or an HLA-A2-negative Right Panel donor was stained with the Alexa Fluor 700 Mouse anti-Human HLA-A2 antibody Cat. No. 561339; solid line histogram or with a Alexa Fluor 700 Mouse IgG2b, kappa Isotype Control Cat. No. 560543; dashed line histogram . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of human HLA-A2 on lymphocytes from HLA-A2-positive and -negative donors. Human whole blood from either an HLA-A2-positive Left Panel or an HLA-A2-negative Right Panel donor was stained with the Alexa Fluor 700 Mouse anti-Human HLA-A2 antibody Cat. No. 561339; solid line histogram or with a Alexa Fluor 700 Mouse IgG2b, kappa Isotype Control Cat. No. 560543; dashed line histogram . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System.