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Flow cytometric analysis of CD31 expression on human peripheral granulocytes. Human whole blood was stained with either Alexa Fluor® 488 Mouse Anti-Human CD31 (Cat. No. 558068; solid line histogram) or Alexa Fluor® 488 Mouse IgG2a, κ Isotype Control (Cat. No. 557703; dashed line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the forward and side light-scattering characteristic of viable granulocytes.
Flow cytometric analysis of CD31 expression on human peripheral granulocytes. Human whole blood was stained with either Alexa Fluor® 488 Mouse Anti-Human CD31 (Cat. No. 558068; solid line histogram) or Alexa Fluor® 488 Mouse IgG2a, κ Isotype Control (Cat. No. 557703; dashed line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the forward and side light-scattering characteristic of viable granulocytes.
Flow cytometric analysis of CD31 expression on human peripheral granulocytes. Human whole blood was stained with either Alexa Fluor® 488 Mouse Anti-Human CD31 (Cat. No. 558068; solid line histogram) or Alexa Fluor® 488 Mouse IgG2a, κ Isotype Control (Cat. No. 557703; dashed line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the forward and side light-scattering characteristic of viable granulocytes.
Flow cytometric analysis of CD31 expression on human peripheral granulocytes. Human whole blood was stained with either Alexa Fluor® 488 Mouse Anti-Human CD31 (Cat. No. 558068; solid line histogram) or Alexa Fluor® 488 Mouse IgG2a, κ Isotype Control (Cat. No. 557703; dashed line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the forward and side light-scattering characteristic of viable granulocytes.
Flow cytometric analysis of CD31 expression on human peripheral granulocytes. Human whole blood was stained with either Alexa Fluor® 488 Mouse Anti-Human CD31 (Cat. No. 558068; solid line histogram) or Alexa Fluor® 488 Mouse IgG2a, κ Isotype Control (Cat. No. 557703; dashed line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the forward and side light-scattering characteristic of viable granulocytes.
Flow cytometric analysis of CD31 expression on human peripheral granulocytes. Human whole blood was stained with either Alexa Fluor® 488 Mouse Anti-Human CD31 (Cat. No. 558068; solid line histogram) or Alexa Fluor® 488 Mouse IgG2a, κ Isotype Control (Cat. No. 557703; dashed line histogram). Erythrocytes were lysed with BD Pharm Lyse™ Lysing Buffer (Cat. No. 555899). Fluorescent histograms were derived from gated events with the forward and side light-scattering characteristic of viable granulocytes.
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The M89D3 monoclonal antibody specifically recognizes CD31, which is also known as platelet endothelial cell adhesion molecule -1 (PECAM-1), a single chain, type I transmembrane protein of approximately 130-140 kDa. CD31 is a member of the immunoglobulin supergene family. Its extracellular region is composed of 574 amino acids and contains six C2-type Ig domains, and the intracellular region is composed of 118 residues. CD31 (PECAM-1) is expressed on endothelial cells, platelets, monocytes, neutrophils and NK cells. It has also been observed on subsets of T cells, but not on circulating B cells. It has been implicated in a number of cellular phenomena, including vascular wound healing, angiogenesis, and transendothelial migration of leukocytes and platelet aggregation in inflammatory responses.
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