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三种转染试剂介导pGPU6/GFP/Neo真核表达载体转染鸡胚成纤维细胞的比较研究 被引量:3

Comparison of three different methods in transfection of plasmid pGPU6/GFP/Neo to chicken embryo fibroblasts
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摘要 目的:采用不同转染试剂介导pGPU6/GFP/Neo质粒转染鸡胚成纤维细胞UMNSAH/DF-1,以获得最优化的方法。方法:分别采用不同剂量(1.25μl、2.0μl、2.5μl)的Lipofectamin2000、Gbfectene-Elite及HilyMax转染试剂介导1μg质粒进行转染,观察其转染效率,测定其转染细胞存活率。结果:HilyMax组的转染效率为(86.85%±2.32%),较Lipofectamin2000组(48.33%±3.24%)、Gbfectene-Elite组(37.35%±5.41%)高(F=18.882,P<0.05);其中,HilyMax 2.5μl组的转染效率最高为(90.53%±1.15%)。Lipofectamin2000组的细胞存活率(65.76%±5.78%)明显低于HilyMax组(89.54%±0.86%)、Gbfectene-Elite组(82.45%±3.56%)(F=90.676,P<0.05)。结论:HilyMax对于鸡胚成纤维细胞具有最好的转染效率和最低的细胞毒性,推荐使用2.5μl HilyMax:1μg质粒进行鸡胚成纤维细胞的转染。 Objective: To compare three different methods in transfection of plasmid pGPU6/GFP/ Neo into chicken embryo fibroblast. Methods: Different doses ( 1.25μl, 2μl, 2.5 μl ) of Lipofectamin2000, Gbfectene-Elite and HilyMax were used to transfect 1μg plasmid pGPU6/GFP/Neo. The transfection efficiency was observed by the fluorescence and the cell viabilities were measured. Results: The transfection efficiency of HilyMax was significant higher than that of Lipofectamin2000 and Gbfectene-Elite(86.85% ± 2. 32% vs 48.33% ± 3.24% and vs 37.35% ± 5.41% ; F = 18. 882, P 〈 0.05). The transfection efficiency of 2. 5μl HilyMax was highest(90. 53% ±1.15% ). The cell viability of Lipofectamin2000 was significantly lower than that of HilyMax and Gbfectene-Elite(65.76% ± 5.78% vs 89.54% ± 0. 86% and vs 82. 45% ± 3.56% ; F = 90. 676, P 〈 0. 05 ). Conclusion : HilyMax has the highest transfection efficiency and the lowest cell toxicity in transfection of plasmid pGPU6/GFP/Neo into chicken embryo fibroblast, with the optimal ratio of 2.5 μl HilyMax : 1 μg plasmid.
出处 《浙江大学学报(医学版)》 CAS CSCD 北大核心 2013年第6期660-665,共6页 Journal of Zhejiang University(Medical Sciences)
基金 浙江省自然科学基金资助项目(Y2110413)
关键词 转染 质粒DNA/遗传学 鸡胚成纤维细胞/细胞学 绿色荧光蛋白质类 细胞毒性 Transfection, plasma/genetics Chicken embryo fibroblast/cytology Green fluorescent protein Cell toxicity
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  • 1EVANS C H, GHIVIZZANI S C, ROBBINS P D. Orthopedic gene therapy in 2008 [ J ]. Mol Ther, 2009,17 (2) :231-244.
  • 2CHALFIE M,TU Y, EUSKIRCHEN G, et al. Green fluorescent protein as a marker for gene expression [ J ]. Science, 1994,263 (5148 ) : 802 - 805.
  • 3TCHURIKOV N A, ZAVILGELSKY G B, MANUKHOV I V, et al. Gene-specific silencing by expression of parallel complementary RNA in Escherichiacoli [ J ]. J Biol Chem, 2000,275 (34) : 26523-26529.
  • 4BOTTEGA R, EPAND RM. Inhibition of protein kinase C by cationic amphiphiles [ J ]. Biochemistry, 1992,31 (37) :9025-9230.
  • 5DATILES M J, JOHNSON E A, MCCARTY R E. Inhibition of the ATPase activity of the catalytic portion of ATP synthases by cationic amphiphiles [ J ]. Biochim Biophys Acta,2008,1777 (4) :362- 328.
  • 6BEAVIS A D. On the inhibition of the mitochondrial inner membrane anion uniporter by cationic amphiphiles and other drtxgs [ J 1. J Biol Chem, 1989,264 ( 3 ) : 1508-1515.
  • 7PANG Junjie, SHI Haiming, LUO Xinping, et al . Comparison of the transfection efficiency of U937 monocytes by different methods [ J ]. Fndan University Journal of Medical Sciences , 201 0, 37 (5) :594-597. ( in Chinese).

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