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Flow cytometric analysis of CD31 expression on rat splenic leukocytes. LEW splenocytes were stained with FITC Mouse Anti-Rat CD45RA (Cat. No. 554883) and Biotin Mouse Anti-Rat CD31 (Cat. No. 555026; Right Panel), followed by PE Streptavidin (Cat. No. 554061). Contour plots were derived from gated events with the side and forward light-scattering characteristics of viable splenocytes. Flow cytometry was performed on a BD FACScan™ system.
Flow cytometric analysis of CD31 expression on rat splenic leukocytes. LEW splenocytes were stained with FITC Mouse Anti-Rat CD45RA (Cat. No. 554883) and Biotin Mouse Anti-Rat CD31 (Cat. No. 555026; Right Panel), followed by PE Streptavidin (Cat. No. 554061). Contour plots were derived from gated events with the side and forward light-scattering characteristics of viable splenocytes. Flow cytometry was performed on a BD FACScan™ system.
Flow cytometric analysis of CD31 expression on rat splenic leukocytes. LEW splenocytes were stained with FITC Mouse Anti-Rat CD45RA (Cat. No. 554883) and Biotin Mouse Anti-Rat CD31 (Cat. No. 555026; Right Panel), followed by PE Streptavidin (Cat. No. 554061). Contour plots were derived from gated events with the side and forward light-scattering characteristics of viable splenocytes. Flow cytometry was performed on a BD FACScan™ system.
Flow cytometric analysis of CD31 expression on rat splenic leukocytes. LEW splenocytes were stained with FITC Mouse Anti-Rat CD45RA (Cat. No. 554883) and Biotin Mouse Anti-Rat CD31 (Cat. No. 555026; Right Panel), followed by PE Streptavidin (Cat. No. 554061). Contour plots were derived from gated events with the side and forward light-scattering characteristics of viable splenocytes. Flow cytometry was performed on a BD FACScan™ system.
Flow cytometric analysis of CD31 expression on rat splenic leukocytes. LEW splenocytes were stained with FITC Mouse Anti-Rat CD45RA (Cat. No. 554883) and Biotin Mouse Anti-Rat CD31 (Cat. No. 555026; Right Panel), followed by PE Streptavidin (Cat. No. 554061). Contour plots were derived from gated events with the side and forward light-scattering characteristics of viable splenocytes. Flow cytometry was performed on a BD FACScan™ system.
Flow cytometric analysis of CD31 expression on rat splenic leukocytes. LEW splenocytes were stained with FITC Mouse Anti-Rat CD45RA (Cat. No. 554883) and Biotin Mouse Anti-Rat CD31 (Cat. No. 555026; Right Panel), followed by PE Streptavidin (Cat. No. 554061). Contour plots were derived from gated events with the side and forward light-scattering characteristics of viable splenocytes. Flow cytometry was performed on a BD FACScan™ system.
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The TLD-3A12 antibody specifically recognizes CD31, also known as PECAM-1 (platelet endothelial cell adhesion molecule). CD31 is a ~130 kDa integral membrane glycoprotein, a member of the immunoglobulin superfamily, that mediates homophilic and heterophilic cell-cell adhesion. CD31 is expressed on endothelial cells, platelets, and subsets of leucocytes. In the human and mouse, multiple alternatively spliced isoforms have been identified, and this alternative splicing may be involved in the regulation of ligand specificity. CD31-mediated endothelial cell-cell interactions are involved in angiogenesis in the mouse and rat. In addition, PECAM-1 has been demonstrated to play an important role in extravasation of leucocytes in vivo, but in vivo treatment with TLD-3A12 mAb had no discernable effect upon the inflammatory infiltrate in experimental allergic encephalomyelitis. The TLD-3A12 mAb partially blocks the proliferative response of antigen-specific CD4+ T cells to antigen-presenting cells and relevant antigen. This mouse anti-rat CD31 antibody crossreacts with pig endothelial cells and platelets, as determined by immunohistochemical staining of acetone-fixed frozen sections and immunofluorescent staining with flow cytometric analysis, respectively. A suspension of Lewis rat microglial cells was used as the the immunogen.
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Global - Refer to manufacturer's instructions for use and related User Manuals and Technical data sheets before using this products as described
Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
Refer to manufacturer's instructions for use and related User Manuals and Technical Data Sheets before using this product as described.
Comparisons, where applicable, are made against older BD technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.