BD Pharmingen- PE-Cy-5 Hamster Anti-Mouse TCR - Chain_BD Pharmingen
参考图片
αβ TCR expression in spleen and thymus. BALB/c splenocytes were simultaneously stained with PE-conjugated anti-mouse CD4 mAb RM4-5 (Cat. No. 553048/553049, left panels), PE-conjugated anti-mouse CD8a mAb 53-6.7 (Cat. No. 553032/553033, left panels), and PE-Cy5-conjugated mAb H57-597 (bottom left panel) monoclonal antibodies, in the presence of Mouse BD Fc Block™ purified anti-mouse CD16/CD32 mAb 2.4G2 (Cat. No. 553141/553142, left panels). BALB/c thymocytes were stained with PE-Cy5-conjugated mAb H57-597 (bottom right panel) or unstained (top right panel). Flow cytometry was performed on a BD FACScan™ flow cytometry system.
Flow cytometric analysis of αβ TCR expression in spleen and thymus. BALB/c splenocytes were simultaneously stained with PE-conjugated anti-mouse CD4 (Cat. No. 553048/553049; left panels), PE Rat Anti-Mouse CD8a (Cat. No. 553032/553033; left panels), and PE-Cy™5 Hamster Anti-Mouse TCR β Chain (Cat. No. 553173; bottom left panel) monoclonal antibodies, in the presence of Purified Rat Anti-Mouse CD16/CD32 (Mouse BD Fc Block™), (Cat. No. 553141/553142; left panels). BALB/c thymocytes were stained with PE-Cy™5 Hamster Anti-Mouse TCR β Chain (bottom right panel) or unstained (top right panel). The fluorescence histograms and contour plots were derived from gated events with the forward and side light-scattering characteristics of viable splenocytes and thymocytes. Flow cytometry was performed on a BD FACScan™.
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