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Flow cytometric analysis of CD11c expression on human peripheral blood lymphocytes (Left Panel) or monocytes (Right Panel). Whole blood was stained with either PE Mouse Anti-Human CD11c (Cat. No. 560999/555392; solid line histogram) or PE Mouse IgG1, κ Isotype Control (Cat. No. 555749; dashed line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms depicting CD11c (or Ig isotype) expression were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes or monocytes. Flow cytometry was performed on a BD FACScan™ system.
Flow cytometric analysis of CD11c expression on human peripheral blood lymphocytes (Left Panel) or monocytes (Right Panel). Whole blood was stained with either PE Mouse Anti-Human CD11c (Cat. No. 560999/555392; solid line histogram) or PE Mouse IgG1, κ Isotype Control (Cat. No. 555749; dashed line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms depicting CD11c (or Ig isotype) expression were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes or monocytes. Flow cytometry was performed on a BD FACScan™ system.
Flow cytometric analysis of CD11c expression on human peripheral blood lymphocytes (Left Panel) or monocytes (Right Panel). Whole blood was stained with either PE Mouse Anti-Human CD11c (Cat. No. 560999/555392; solid line histogram) or PE Mouse IgG1, κ Isotype Control (Cat. No. 555749; dashed line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms depicting CD11c (or Ig isotype) expression were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes or monocytes. Flow cytometry was performed on a BD FACScan™ system.
Flow cytometric analysis of CD11c expression on human peripheral blood lymphocytes (Left Panel) or monocytes (Right Panel). Whole blood was stained with either PE Mouse Anti-Human CD11c (Cat. No. 560999/555392; solid line histogram) or PE Mouse IgG1, κ Isotype Control (Cat. No. 555749; dashed line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms depicting CD11c (or Ig isotype) expression were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes or monocytes. Flow cytometry was performed on a BD FACScan™ system.
Flow cytometric analysis of CD11c expression on human peripheral blood lymphocytes (Left Panel) or monocytes (Right Panel). Whole blood was stained with either PE Mouse Anti-Human CD11c (Cat. No. 560999/555392; solid line histogram) or PE Mouse IgG1, κ Isotype Control (Cat. No. 555749; dashed line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms depicting CD11c (or Ig isotype) expression were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes or monocytes. Flow cytometry was performed on a BD FACScan™ system.
Flow cytometric analysis of CD11c expression on human peripheral blood lymphocytes (Left Panel) or monocytes (Right Panel). Whole blood was stained with either PE Mouse Anti-Human CD11c (Cat. No. 560999/555392; solid line histogram) or PE Mouse IgG1, κ Isotype Control (Cat. No. 555749; dashed line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms depicting CD11c (or Ig isotype) expression were derived from gated events with the side and forward light-scattering characteristics of viable lymphocytes or monocytes. Flow cytometry was performed on a BD FACScan™ system.
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The B-ly6 monoclonal antibody specifically binds to the 150 kDa adhesion glycoprotein CD11c (p150, integrin α chain). CD11c is expressed on dendritic cells, monocytes, macrophages, granulocytes, NK cells and subsets of B and T cells. It associates with CD18 to form the CD11c/CD18 complex that binds fibrinogen and has been reported to be a receptor for iC3b and ICAM-1. Reports indicate that CD11c/CD18 plays a role as an adhesion molecule that mediates cellular binding to ligands expressed on stimulated epithelium and endothelium.
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