参考图片
The expression ICOS on activated T lymphocytes. BALB/c splenocytes were either unstimulated (top panels) or activated by culture for 48 hours in the presence of soluble 145-2C11 mAb (anti-mouse CD3e, Cat. No. 553057, bottom panels). Both sets of cells were stained with either PE-conjugated rat IgG2b, κ isotype control mAb A95-1 (Cat. No. 553989, left panels) or PE-conjugated mAb 7E.17G9 (right panels), then FITC-conjugated mAb 53-6.7 (anti-mouse CD8a, Cat. No. 553030/553031). Viable leukocytes were selected by exclusion of propidium iodide. Flow cytometry was performed on a FACSCalibur™ (BD Biosciences, San Jose, CA).
The expression ICOS on activated T lymphocytes. BALB/c splenocytes were either unstimulated (top panels) or activated by culture for 48 hours in the presence of soluble 145-2C11 mAb (anti-mouse CD3e, Cat. No. 553057, bottom panels). Both sets of cells were stained with either PE-conjugated rat IgG2b, κ isotype control mAb A95-1 (Cat. No. 553989, left panels) or PE-conjugated mAb 7E.17G9 (right panels), then FITC-conjugated mAb 53-6.7 (anti-mouse CD8a, Cat. No. 553030/553031). Viable leukocytes were selected by exclusion of propidium iodide. Flow cytometry was performed on a FACSCalibur™ (BD Biosciences, San Jose, CA).
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