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Hepa1-6细胞的最佳培养条件研究
引用本文:杨慈清,李小英.Hepa1-6细胞的最佳培养条件研究[J].安徽农业科学,2010,38(28):15507-15509.
作者姓名:杨慈清  李小英
作者单位:新乡医学院生命科学技术系,河南新乡,453003;新乡医学院生命科学技术系,河南新乡,453003
摘    要:目的]探索Hepa1-6细胞的最佳培养条件。方法]以小鼠Hepa1-6肝癌细胞为材料,采用正交试验设计研究RPMI1640和DMEM2种不同培养基及细胞接种密度、血清浓度、双抗浓度、D-Hanks漂洗次数、胰蛋白酶浓度和消化时间6个不同因素对Hepa1-6传代培养的影响;根据细胞在6个时间点的生长状况评分,筛选出Hepa1-6细胞的最佳培养条件。结果]Hepa1-6细胞在含有20%血清的RPMI-1640培养基,接种密度为4×104个/cm2,100U/ml的双抗浓度,贴壁率在90%以上时,D-Hanks漂洗1次,0.5%胰蛋白酶消化2min,传代效果最好。结论]通过正交设计筛选,为Hepa1-6细胞体外培养探索出最佳培养条件。

关 键 词:Hepa1-6细胞  正交设计  细胞培养

Study on the Optimum Culture Conditions of Hepal-6 Cells
Institution:YANG Ci-qing et al ( Department of Life Science and Technique, Xinxiang Medical University, Xinxiang, Henan 453003 )
Abstract:Objective]The research aimed to explore the optimum culture conditions of Hepa1-6 cells.Method] Hepa1-6 hepatoma cell lines of mice were used to make the orthogonal test.The effects of RPMI1640 and DMEM media,cell inoculation density,serum concentrations,penicillin and streptomycin concentration,the times of washing by D-Hanks,digestion time and concentration of trypsin on the passage culture of Hepa1-6 cells were studied.Based on the growth situations of cells at 6 time points,the optimum culture conditions of Hepa1-6 cells were screened out.Result]Hepa1-6 cells grew well in the RPMI-1640 medium that contained 20% serum,and inoculation density was 4×104 cell/cm2,penicillin and streptomycin concentration of 100 U/ml.It’s have good digest effect that D-Hanks was used to wash the cells once,0.5% trypsin was digested for 2 min when the convergence rate was more than 90% .Conclusion]Through the orthogonal design,the optimum culture conditions of Hepa1-6 cells in vitro were explored.
Keywords:Hepal-6 cells  Orthogonal design  Cell culture
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