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Flow cytometric analysis of expression of CD18 on peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD18 (Cat. No. 551060; solid line histogram) or with an APC Mouse IgG1, κ Isotype Control (Cat. No. 555751; dashed line histogram). The erythrocytes were lysed with Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphocytes.
Flow cytometric analysis of expression of CD18 on peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD18 (Cat. No. 551060; solid line histogram) or with an APC Mouse IgG1, κ Isotype Control (Cat. No. 555751; dashed line histogram). The erythrocytes were lysed with Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphocytes.
Flow cytometric analysis of expression of CD18 on peripheral blood lymphocytes. Whole blood was stained with APC Mouse Anti-Human CD18 (Cat. No. 551060; solid line histogram) or with an APC Mouse IgG1, κ Isotype Control (Cat. No. 555751; dashed line histogram). The erythrocytes were lysed with Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from gated events with the forward and side light-scattering characteristics of viable lymphocytes.
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The 6.7 monoclonal antibody specifically binds to β2 integrin, a 90-95 kDa transmembrane protein, which associates non-covalently as a heterodimer with the a chains of CD11a, CD11b, or CD11c. CD18 is expressed on lymphocytes, monocytes, and more weakly on granulocytes. LFA-1 has been shown to play an important role in homotypic and heterotypic cellular adhesion in immune and inflammatory responses.
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