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作 者:张宝[1,2] 霍霞[1] 徐锡金[1] 齐宗利[1] 郑谨[1] 彭琳[1]
机构地区:[1]汕头大学医学院中心实验室,广东省免疫病理学重点实验室 [2]南方医科大学生物化学教研室,广东广州510515
出 处:《生物技术通讯》2007年第4期638-640,共3页Letters in Biotechnology
基 金:中国博士后科学基金项目(2005038187)
摘 要:目的:比较LipofectAMINE2000与Fugene6转染细胞的效果。方法:将含有Firefly和Renilla荧光素酶基因的质粒分别用LipofectAMINE2000和Fugene6转染293T、HepG2和DLD-1细胞,于48h后裂解细胞测定荧光素酶活性。结果:在293T细胞中,LipofectAMINE2000转染组的萤火虫(Firefly)和Renilla荧光素酶活性分别是Fugene6转染组的6.5和5.6倍(P<0.005);在HepG2细胞中,LipofectAMINE2000转染组的Firefly和Renilla荧光素酶活性分别是Fugene6转染组的44和49倍(P<0.001);而在DLD-1细胞中,两者无差别。结论:转染试剂LipofectAMINE2000和Fugene6对不同细胞的转染效果存在差异,当进行转染实验时,对于不同的细胞须根据情况进行选择。Objective: To compare the transfection efficiency of LipofectAMINE2000 and Fugene6. Methods: The plasmids containing the Firefly luciferase and Renilla luciferase gene were transfected into 293T, HepG2, DLD-1 cells using LipofectAMINE2000 and Fugene6 respectively. After 48 h transfection, ceils were lysed and the luciferase activity was detected. Results: In 293T cells, the Firefly and Renilla luciferase activity of LipofectAMINE2000 transfection group were as more 6.5, 5.6 fold as that of Fugene6 transfection group (P〈O.005); while in HepG2 cells, the activity of LipofectAMINE2000 transfection group were as more 44, 49 times as Fugene6 transfection group (P〈O.001); but in DLD-1 cells, there was no difference between two groups. Conclusion: There is significant difference between LipofectAMINE2000 and Fugene6 for transfecting different cells. That might be needed to choose proper transfection agents depending on the type of cells.
关 键 词:LipofectAMINE2000 Fugene6 转染
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