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Flow cytometric analysis of CD20 expression on human peripheral blood lymphocytes. Whole blood was stained with either Alexa Fluor 700 Mouse IgG2b, κ Isotype Control (Cat. No. 560543; dashed line histogram) or Alexa Fluor 700 Mouse Anti-Human CD20 (Cat. No. 560631; solid line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD™ LSR II flow cytometry system.
Flow cytometric analysis of CD20 expression on human peripheral blood lymphocytes. Whole blood was stained with either Alexa Fluor 700 Mouse IgG2b, κ Isotype Control (Cat. No. 560543; dashed line histogram) or Alexa Fluor 700 Mouse Anti-Human CD20 (Cat. No. 560631; solid line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD™ LSR II flow cytometry system.
Flow cytometric analysis of CD20 expression on human peripheral blood lymphocytes. Whole blood was stained with either Alexa Fluor 700 Mouse IgG2b, κ Isotype Control (Cat. No. 560543; dashed line histogram) or Alexa Fluor 700 Mouse Anti-Human CD20 (Cat. No. 560631; solid line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD™ LSR II flow cytometry system.
Flow cytometric analysis of CD20 expression on human peripheral blood lymphocytes. Whole blood was stained with either Alexa Fluor 700 Mouse IgG2b, κ Isotype Control (Cat. No. 560543; dashed line histogram) or Alexa Fluor 700 Mouse Anti-Human CD20 (Cat. No. 560631; solid line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD™ LSR II flow cytometry system.
Flow cytometric analysis of CD20 expression on human peripheral blood lymphocytes. Whole blood was stained with either Alexa Fluor 700 Mouse IgG2b, κ Isotype Control (Cat. No. 560543; dashed line histogram) or Alexa Fluor 700 Mouse Anti-Human CD20 (Cat. No. 560631; solid line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD™ LSR II flow cytometry system.
Flow cytometric analysis of CD20 expression on human peripheral blood lymphocytes. Whole blood was stained with either Alexa Fluor 700 Mouse IgG2b, κ Isotype Control (Cat. No. 560543; dashed line histogram) or Alexa Fluor 700 Mouse Anti-Human CD20 (Cat. No. 560631; solid line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes. Flow cytometry was performed on a BD™ LSR II flow cytometry system.
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The 2H7 monoclonal antibody specifically binds to CD20, encoded by the MS4A1 (Membrane-spanning 4-domains, subfamily A, member 1) gene. CD20 is a 33-37 kDa, unglycosylated four-transmembrane phosphoprotein. CD20 is expressed on pre-B-cells, resting and activated B cells, and follicular dendritic cells, but not plasma cells. Low level CD20 expression is observed on a small subset of normal circulating T lymphocytes. The CD20 molecule is involved in the regulation of B-cell activation.
This clone also cross-reacts with a subset of peripheral blood lymphocytes, but not monocytes nor granulocytes, of baboon and both rhesus and cynomolgus macaque monkeys. The distribution on lymphocytes is similar to that seen with normal human donor lymphocytes, namely bright staining on B lymphocytes and weak reactivity on a small subset of CD3-positive T lymphocytes.
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