BD HorizonTM V450 Mouse Anti-NHP CD45

Description

Flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with BD Horizon V450 Mouse anti-NHP CD45 antibody Cat. No. 561291; Right Panel or with a BD Horizon V450 Mouse IgG1, kappa Isotype Control Cat. No. 560373; Left Panel . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two parameter flow cytometric dot blots showing the correlated expression of CD45 or Ig Isotype control staining versus side-scattered light signals were derived from events with the forward light scatter signals of viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with BD Horizon V450 Mouse anti-NHP CD45 antibody Cat. No. 561291; Right Panel or with a BD Horizon V450 Mouse IgG1, kappa Isotype Control Cat. No. 560373; Left Panel . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two parameter flow cytometric dot blots showing the correlated expression of CD45 or Ig Isotype control staining versus side-scattered light signals were derived from events with the forward light scatter signals of viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with BD Horizon V450 Mouse anti-NHP CD45 antibody Cat. No. 561291; Right Panel or with a BD Horizon V450 Mouse IgG1, kappa Isotype Control Cat. No. 560373; Left Panel . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two parameter flow cytometric dot blots showing the correlated expression of CD45 or Ig Isotype control staining versus side-scattered light signals were derived from events with the forward light scatter signals of viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with BD Horizon V450 Mouse anti-NHP CD45 antibody Cat. No. 561291; Right Panel or with a BD Horizon V450 Mouse IgG1, kappa Isotype Control Cat. No. 560373; Left Panel . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two parameter flow cytometric dot blots showing the correlated expression of CD45 or Ig Isotype control staining versus side-scattered light signals were derived from events with the forward light scatter signals of viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with BD Horizon V450 Mouse anti-NHP CD45 antibody Cat. No. 561291; Right Panel or with a BD Horizon V450 Mouse IgG1, kappa Isotype Control Cat. No. 560373; Left Panel . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two parameter flow cytometric dot blots showing the correlated expression of CD45 or Ig Isotype control staining versus side-scattered light signals were derived from events with the forward light scatter signals of viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with BD Horizon V450 Mouse anti-NHP CD45 antibody Cat. No. 561291; Right Panel or with a BD Horizon V450 Mouse IgG1, kappa Isotype Control Cat. No. 560373; Left Panel . The erythrocytes were lysed with BD PharmLyse Lysing Buffer Cat. No. 555899 . Two parameter flow cytometric dot blots showing the correlated expression of CD45 or Ig Isotype control staining versus side-scattered light signals were derived from events with the forward light scatter signals of viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System.