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作 者:苏玲[1] 李雨婷[1] 王再林[1] 宋慧[1] 杜金[1] 吴宗翰[1] 张中北[1]
出 处:《吉林大学学报(理学版)》2013年第1期140-144,共5页Journal of Jilin University:Science Edition
基 金:吉林省世行贷款农产品质量安全项目(批准号:2011-Y18)
摘 要:应用胺化还原法在树舌灵芝液体深层发酵浸膏水提多糖(GAP)的还原性末端连接荧光基团(FITC),制备荧光标记GAP(FITC-GAP),并测定其荧光取代率为0.90%.利用xCELLigence RTCA DP全自动实时细胞分析仪检测GAP荧光标记,其前后的细胞毒活性不变.流式细胞仪和荧光显微镜对GAP在人大肠癌细胞SWWC1116定位结果表明,GAP可与人大肠癌细胞SWWC1116的细胞膜结合,并可转运至细胞核内.The reductive amination method was used for the fluorescently labelling of Ganoderma aDDlanatum polysaccharide(GAP). FITC was linked up with the reducibility termination of GAP, and fluorescent substitute ratio was determined to be 0.90%. The results of the measurement by xCELLigence RTCA DP automatic real-time cell analyzer show in vitro the cytotoxie activity did not significantly change before and after fluorescent labeling of GAP. The results measured by means of flow cytometer and fluorescence microscope show fluorescence signal was detected both on the cell membrane and in the nucleus, illustrating that GAP can be attached to human colorectal cancer SWWCl116 membrane, and can be further transported to the nuclei.
关 键 词:树舌 多糖 荧光标记 大肠癌细胞SWWClll6 细胞定位
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