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BD HorizonTM BV421 Mouse Anti-Human CD132
GENERAL CATALOGUE

BD HorizonTM BV421 Mouse Anti-Human CD132

562881 · 50 Tests

BDB Bioscience · Cat: 562881

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Catalog No: 562881
Category: reagents
Pack Size: 50 Tests
Brand: BDB Bioscience

Description

Flow cytometric analysis of CD132 expression on human peripheral blood mononuclear cells. Human peripheral blood mononuclear cells were stained with either a BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; dashed line histogram or with BD Horizon BV421 Mouse Anti-Human CD132 antibody Cat. No. 562881/566222; solid line histogram . 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. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD132 expression on human peripheral blood mononuclear cells. Human peripheral blood mononuclear cells were stained with either a BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; dashed line histogram or with BD Horizon BV421 Mouse Anti-Human CD132 antibody Cat. No. 562881/566222; solid line histogram . 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. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD132 expression on human peripheral blood mononuclear cells. Human peripheral blood mononuclear cells were stained with either a BD Horizon BV421 Mouse IgG1, kappa Isotype Control Cat. No. 562438; dashed line histogram or with BD Horizon BV421 Mouse Anti-Human CD132 antibody Cat. No. 562881/566222; solid line histogram . 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. Flow cytometry was performed using a BD LSR II Flow Cytometer System.

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