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Flow cytometric analysis of CD11c on human peripheral lymphocytes and monocytes. Human whole blood was stained with the Alexa Fluor® 700 Mouse anti-Human CD11c antibody (Cat. No. 561352; solid line histogram) or with an Alexa Fluor® 700 Mouse IgG1, κ Isotype Control (Cat. No. 557882; dashed line histogram). The erythrocytes were lysed with BD PharmLyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes (Left Panel) or monocytes (Right Panel). Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of CD11c on human peripheral lymphocytes and monocytes. Human whole blood was stained with the Alexa Fluor® 700 Mouse anti-Human CD11c antibody (Cat. No. 561352; solid line histogram) or with an Alexa Fluor® 700 Mouse IgG1, κ Isotype Control (Cat. No. 557882; dashed line histogram). The erythrocytes were lysed with BD PharmLyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes (Left Panel) or monocytes (Right Panel). Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of CD11c on human peripheral lymphocytes and monocytes. Human whole blood was stained with the Alexa Fluor® 700 Mouse anti-Human CD11c antibody (Cat. No. 561352; solid line histogram) or with an Alexa Fluor® 700 Mouse IgG1, κ Isotype Control (Cat. No. 557882; dashed line histogram). The erythrocytes were lysed with BD PharmLyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes (Left Panel) or monocytes (Right Panel). Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of CD11c on human peripheral lymphocytes and monocytes. Human whole blood was stained with the Alexa Fluor® 700 Mouse anti-Human CD11c antibody (Cat. No. 561352; solid line histogram) or with an Alexa Fluor® 700 Mouse IgG1, κ Isotype Control (Cat. No. 557882; dashed line histogram). The erythrocytes were lysed with BD PharmLyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes (Left Panel) or monocytes (Right Panel). Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of CD11c on human peripheral lymphocytes and monocytes. Human whole blood was stained with the Alexa Fluor® 700 Mouse anti-Human CD11c antibody (Cat. No. 561352; solid line histogram) or with an Alexa Fluor® 700 Mouse IgG1, κ Isotype Control (Cat. No. 557882; dashed line histogram). The erythrocytes were lysed with BD PharmLyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes (Left Panel) or monocytes (Right Panel). Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of CD11c on human peripheral lymphocytes and monocytes. Human whole blood was stained with the Alexa Fluor® 700 Mouse anti-Human CD11c antibody (Cat. No. 561352; solid line histogram) or with an Alexa Fluor® 700 Mouse IgG1, κ Isotype Control (Cat. No. 557882; dashed line histogram). The erythrocytes were lysed with BD PharmLyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes (Left Panel) or monocytes (Right Panel). Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of CD11c on human peripheral lymphocytes and monocytes. Human whole blood was stained with the Alexa Fluor® 700 Mouse anti-Human CD11c antibody (Cat. No. 561352; solid line histogram) or with an Alexa Fluor® 700 Mouse IgG1, κ Isotype Control (Cat. No. 557882; dashed line histogram). The erythrocytes were lysed with BD PharmLyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes (Left Panel) or monocytes (Right Panel). Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of CD11c on human peripheral lymphocytes and monocytes. Human whole blood was stained with the Alexa Fluor® 700 Mouse anti-Human CD11c antibody (Cat. No. 561352; solid line histogram) or with an Alexa Fluor® 700 Mouse IgG1, κ Isotype Control (Cat. No. 557882; dashed line histogram). The erythrocytes were lysed with BD PharmLyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes (Left Panel) or monocytes (Right Panel). Flow cytometry was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of CD11c on human peripheral lymphocytes and monocytes. Human whole blood was stained with the Alexa Fluor® 700 Mouse anti-Human CD11c antibody (Cat. No. 561352; solid line histogram) or with an Alexa Fluor® 700 Mouse IgG1, κ Isotype Control (Cat. No. 557882; dashed line histogram). The erythrocytes were lysed with BD PharmLyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from events with the forward and side light-scatter characteristics of viable lymphocytes (Left Panel) or monocytes (Right Panel). Flow cytometry was performed using a BD™ LSR II Flow Cytometer 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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For Research Use Only. Not for use in diagnostic or therapeutic procedures.