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参考图片
Two-color analysis of the expression of CD73 on splenic T and B lymphocytes. C57BL/6 splenocytes were stained with either purified isotype control mAb R35-95 (Cat. No. 553927, left panel) or purified mAb TY/23 (middle and right panels) followed by biotinylated anti-rat IgG2a mAb RG7/1.30 (Cat. No. 553894), then Streptavidin-PE (Cat. No. 554061). T or B lymphocytes were identified by staining with FITC-conjugated anti-mouse CD3e mAb 145-2C11 (Cat. No. 553061/553062, left and middle panels) or FITC-conjugated anti-mouse CD19 mAb 1D3 (Cat. No. 557398/553785, right panel), respectively. Flow cytometry was performed on a BD FACSCalibur™ flow cytometry system.
Two-color analysis of the expression of CD73 on splenic T and B lymphocytes. C57BL/6 splenocytes were stained with either purified isotype control mAb R35-95 (Cat. No. 553927, left panel) or purified mAb TY/23 (middle and right panels) followed by biotinylated anti-rat IgG2a mAb RG7/1.30 (Cat. No. 553894), then Streptavidin-PE (Cat. No. 554061). T or B lymphocytes were identified by staining with FITC-conjugated anti-mouse CD3e mAb 145-2C11 (Cat. No. 553061/553062, left and middle panels) or FITC-conjugated anti-mouse CD19 mAb 1D3 (Cat. No. 557398/553785, right panel), respectively. Flow cytometry was performed on a BD FACSCalibur™ flow cytometry system.
Two-color analysis of the expression of CD73 on splenic T and B lymphocytes. C57BL/6 splenocytes were stained with either purified isotype control mAb R35-95 (Cat. No. 553927, left panel) or purified mAb TY/23 (middle and right panels) followed by biotinylated anti-rat IgG2a mAb RG7/1.30 (Cat. No. 553894), then Streptavidin-PE (Cat. No. 554061). T or B lymphocytes were identified by staining with FITC-conjugated anti-mouse CD3e mAb 145-2C11 (Cat. No. 553061/553062, left and middle panels) or FITC-conjugated anti-mouse CD19 mAb 1D3 (Cat. No. 557398/553785, right panel), respectively. Flow cytometry was performed on a BD FACSCalibur™ flow cytometry system.
