BD Pharmingen- PerCP Hamster Anti-Mouse CD3e_BD Pharmingen
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CD3e expression in spleen and thymus. BALB/c splenocytes were simultaneously stained with PE-conjugated anti-mouse CD4 mAb RM4-5 (Cat. No. 553049), PE-conjugated anti-mouse CD8a mAb 53-6.7 (Cat. No. 553033) and PerCP-conjugated anti-mouse CD3e mAb 145-2C11 (bottom left panel). BALB/c thymocytes were also stained with PerCP-conjugated mAb 145-2C11 (bottom right panel) or were unstained (top right panel). Flow cytometry was performed on a BD FACScan™ flow cytometry system.
Multicolor flow cytometric analysis of CD3e expression on mouse splenocytes. Mouse splenic leucocytes were stained with FITC Rat Anti-Mouse CD4 (Cat. No.553046/553047/561835), FITC Rat Anti-Mouse CD8a (Cat. No. 553030/553031/561966) and either PerCP Armenian Hamster IgG1, κ Isotype Control (Cat. No. 553975; Left Plot) or PerCP Hamster Anti-Mouse CD3e antibodies (Cat. No. 553067/ 561089; Right Plot) at 0.5 µg/test. Bivariate pseudocolor density plots showing the correlated expression of CD3e (or Ig Isotype Control staining) versus CD4 and CD8a were derived from gated events with the forward and side light-scatter characteristics of splenic leucocytes. Flow cytometry and data analysis were performed using a BD FACSCanto II™ Cell Analyzer System and FlowJo™ software. Data shown on this Technical Data Sheet are not lot specific.
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