
563126 ·
BDB Bioscience · Cat: 563126
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bdbiosciences.com/en-us/products/reagents/flow-cytometry-rea...Description
Multicolor flow cytometric analysis of CD20 expression on human peripheral blood lymphocytes. Whole blood was stained with either BD Horizon BV711 Mouse IgG2b, kappa Isotype Control Cat. No. 563125; Left Panel or with BD Horizon BV711 Mouse Anti-Human CD20 antibody Cat. No. 563126; Right Panel . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two color flow cytometric dot plots show the correlated expression of CD20 or Ig Isotype Control staining versus cellular autofluorescence derived from gated events with the forward light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD20 expression on human peripheral blood lymphocytes. Whole blood was stained with either BD Horizon BV711 Mouse IgG2b, kappa Isotype Control Cat. No. 563125; Left Panel or with BD Horizon BV711 Mouse Anti-Human CD20 antibody Cat. No. 563126; Right Panel . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two color flow cytometric dot plots show the correlated expression of CD20 or Ig Isotype Control staining versus cellular autofluorescence derived from gated events with the forward light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD20 expression on human peripheral blood lymphocytes. Whole blood was stained with either BD Horizon BV711 Mouse IgG2b, kappa Isotype Control Cat. No. 563125; Left Panel or with BD Horizon BV711 Mouse Anti-Human CD20 antibody Cat. No. 563126; Right Panel . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two color flow cytometric dot plots show the correlated expression of CD20 or Ig Isotype Control staining versus cellular autofluorescence derived from gated events with the forward light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Multicolor flow cytometric analysis of CD20 expression on human peripheral blood lymphocytes. Whole blood was stained with either BD Horizon BV711 Mouse IgG2b, kappa Isotype Control Cat. No. 563125; Left Panel or with BD Horizon BV711 Mouse Anti-Human CD20 antibody Cat. No. 563126; Right Panel . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two color flow cytometric dot plots show the correlated expression of CD20 or Ig Isotype Control staining versus cellular autofluorescence derived from gated events with the forward light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Show More Multicolor flow cytometric analysis of CD20 expression on human peripheral blood lymphocytes. Whole blood was stained with either BD Horizon BV711 Mouse IgG2b, kappa Isotype Control Cat. No. 563125; Left Panel or with BD Horizon BV711 Mouse Anti-Human CD20 antibody Cat. No. 563126; Right Panel . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two color flow cytometric dot plots show the correlated expression of CD20 or Ig Isotype Control staining versus cellular autofluorescence derived from gated events with the forward light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System. Multicolor flow cytometric analysis of CD20 expression on human peripheral blood lymphocytes. Whole blood was stained with either BD Horizon BV711 Mouse IgG2b, kappa Isotype Control Cat. No. 563125; Left Panel or with BD Horizon BV711 Mouse Anti-Human CD20 antibody Cat. No. 563126; Right Panel . Erythrocytes were lysed with BD Pharm Lyse Lysing Buffer Cat. No. 555899 . Two color flow cytometric dot plots show the correlated expression of CD20 or Ig Isotype Control staining versus cellular autofluorescence derived from gated events with the forward light-scatter characteristics of viable lymphocytes. Flow cytometry was performed using a BD LSR II Flow Cytometer System.