BD PharmingenTM Purified NA/LE Mouse Anti-Human CD2

Description

Flow cytometric analysis of CD2 expression on rhesus macaque Macaca mulatta peripheral blood lymphocytes. Whole blood was stained with either Purified NA/LE Mouse IgG1 kappa Isotype Control Cat. No. 554721; dashed line histogram or Purified NA/LE Mouse Anti-Human CD2 Cat. No. 555323; solid line histogram . Secondary staining was carried out with FITC Goat Anti-Mouse IgG/IgM Cat. No. 555988 and erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . The fluorescence histograms showing CD2 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometry was carried out on a BD FACScan system. Flow cytometric analysis of CD2 expression on rhesus macaque Macaca mulatta peripheral blood lymphocytes. Whole blood was stained with either Purified NA/LE Mouse IgG1 kappa Isotype Control Cat. No. 554721; dashed line histogram or Purified NA/LE Mouse Anti-Human CD2 Cat. No. 555323; solid line histogram . Secondary staining was carried out with FITC Goat Anti-Mouse IgG/IgM Cat. No. 555988 and erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . The fluorescence histograms showing CD2 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometry was carried out on a BD FACScan system. Show More Flow cytometric analysis of CD2 expression on rhesus macaque Macaca mulatta peripheral blood lymphocytes. Whole blood was stained with either Purified NA/LE Mouse IgG1 kappa Isotype Control Cat. No. 554721; dashed line histogram or Purified NA/LE Mouse Anti-Human CD2 Cat. No. 555323; solid line histogram . Secondary staining was carried out with FITC Goat Anti-Mouse IgG/IgM Cat. No. 555988 and erythrocytes were lysed with BD FACS Lysing Solution Cat. No. 349202 . The fluorescence histograms showing CD2 expression or Ig Isotype control staining were derived from gated events with the forward and side light-scatter characteristics of intact lymphocytes. Flow cytometry was carried out on a BD FACScan system.