

561489 ·
BDB Bioscience · Cat: 561489
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bdbiosciences.com/en-us/products/reagents/flow-cytometry-rea...Description
Multiparameter flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with a BD Horizon V500 Mouse IgG1, kappa Isotype Control Cat. No. 560787; Left Panel or with BD Horizon V500 Mouse Anti-NHP CD45 antibody Cat. No. 561489; Right 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 characteristics were derived from events gated for all viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multiparameter flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with a BD Horizon V500 Mouse IgG1, kappa Isotype Control Cat. No. 560787; Left Panel or with BD Horizon V500 Mouse Anti-NHP CD45 antibody Cat. No. 561489; Right 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 characteristics were derived from events gated for all viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multiparameter flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with a BD Horizon V500 Mouse IgG1, kappa Isotype Control Cat. No. 560787; Left Panel or with BD Horizon V500 Mouse Anti-NHP CD45 antibody Cat. No. 561489; Right 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 characteristics were derived from events gated for all viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Multiparameter flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with a BD Horizon V500 Mouse IgG1, kappa Isotype Control Cat. No. 560787; Left Panel or with BD Horizon V500 Mouse Anti-NHP CD45 antibody Cat. No. 561489; Right 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 characteristics were derived from events gated for all viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Multiparameter flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with a BD Horizon V500 Mouse IgG1, kappa Isotype Control Cat. No. 560787; Left Panel or with BD Horizon V500 Mouse Anti-NHP CD45 antibody Cat. No. 561489; Right 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 characteristics were derived from events gated for all viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multiparameter flow cytometric analysis of CD45 expression on Rhesus macaque peripheral blood leukocytes. Rhesus macaque whole blood was stained with a BD Horizon V500 Mouse IgG1, kappa Isotype Control Cat. No. 560787; Left Panel or with BD Horizon V500 Mouse Anti-NHP CD45 antibody Cat. No. 561489; Right 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 characteristics were derived from events gated for all viable leukocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System.