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成肌细胞体外培养中两种纯化方法的比较
引用本文:谢艳,朱太咏,赵东亮. 成肌细胞体外培养中两种纯化方法的比较[J]. 中医药导报, 2008, 14(12): 69-70
作者姓名:谢艳  朱太咏  赵东亮
作者单位:河南省正骨研究院,河南洛阳,471002
基金项目:河南省科技攻关项目(991170632)
摘    要:
目的:比较成肌细胞体外培养中两种纯化方法的优劣。方法:将鸡胚成肌细胞进行体外培养,分别用差速贴壁法和Percoll液梯度离心法纯化成肌细胞。每组培养皿中放置3块盖玻片。每天观察两组细胞的增殖情况,细胞贴壁后第7d更换融合培养基,继续培养6d,取出盖玻片进行HE染色,观察细胞融合情况。结果:两组细胞都有融合,但梯度离心法纯化后培养的细胞融合率较贴壁组高,差异有统计学意义(P〈0.01)。结论:梯度离心法纯化的成肌细胞培养后细胞纯度更高,建议用此法进行成肌细胞的纯化。

关 键 词:成肌细胞  纯化  差速贴壁法  Percoll梯度离心法

The Comparison of Two Purification in Myoblasts Culture
XIE Yan,ZHU Tai-yong,ZHAO Dong-liang. The Comparison of Two Purification in Myoblasts Culture[J]. GUIDING JOURNAL OF TCM, 2008, 14(12): 69-70
Authors:XIE Yan  ZHU Tai-yong  ZHAO Dong-liang
Abstract:
Objective:To compare the advantage and disadvantage of two different purification in myoblasts culture. Methods: Myoblasts of chick embryo were cultured in vitro. Purifying the myoblasts by differential adhesion or Percoll density gradient centrifugation. Laying three cover slips in each culture dish and observing proliferation behavior of myoblasts every day. The syncretic medium was added in culture dish in seven days after adhesion of myoblasts and then culture was kept on for 6 days. Cover slips were ta...
Keywords:Myoblast  Purification  Differential Adhesion  Percoll Gradient Centrifugation  
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