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Flow cytometric analysis of CD22 expression on human peripheral blood lymphocytes. Whole blood was stained with PE Mouse Anti-Human CD22 antibody (Cat. No. 562859; solid line histogram) or PE Mouse IgG1, κ Isotype Control (Cat. No. 554680; dashed line histogram). Erythrocytes were lysed with BD PharmLyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of CD22 expression on human peripheral blood lymphocytes. Whole blood was stained with PE Mouse Anti-Human CD22 antibody (Cat. No. 562859; solid line histogram) or PE Mouse IgG1, κ Isotype Control (Cat. No. 554680; dashed line histogram). Erythrocytes were lysed with BD PharmLyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.
Flow cytometric analysis of CD22 expression on human peripheral blood lymphocytes. Whole blood was stained with PE Mouse Anti-Human CD22 antibody (Cat. No. 562859; solid line histogram) or PE Mouse IgG1, κ Isotype Control (Cat. No. 554680; dashed line histogram). Erythrocytes were lysed with BD PharmLyse™ Lysing Buffer (Cat. No. 555899). The fluorescence histograms were derived from gated events with the forward and side light-scatter characteristics of viable lymphocytes. Flow cytometric analysis was performed using a BD™ LSR II Flow Cytometer System.
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The HIB22 monoclonal antibody specifically binds to CD22. CD22 is a 130-140 kDa glycosylated type I integral membrane protein present on the surface of mature B cells. CD22 is expressed in the cytoplasm of virtually all B cells except plasma cells. CD45RO antigen on T cells and CD75 antigen on B cells have been identified as ligands for CD22. CD22 has been reported to participate in B-cell activation and also as an adhesion molecule. Although the immunobiology of this antigen has not been fully elucidated, reports indicate that ligation of CD22 induces constitutive internalization of the molecule followed by complete degradation.
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