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鸡MyoG基因在成纤维细胞中的表达
引用本文:张婷婷,胡兰,王宏艳,袁亚琦,郝文博,杨晓宇.鸡MyoG基因在成纤维细胞中的表达[J].东北农业大学学报,2010,41(3).
作者姓名:张婷婷  胡兰  王宏艳  袁亚琦  郝文博  杨晓宇
作者单位:沈阳农业大学畜牧兽医学院,沈阳,110161;沈阳农业大学畜牧兽医学院,沈阳,110161;沈阳农业大学畜牧兽医学院,沈阳,110161;沈阳农业大学畜牧兽医学院,沈阳,110161;沈阳农业大学畜牧兽医学院,沈阳,110161;沈阳农业大学畜牧兽医学院,沈阳,110161
基金项目:辽宁省教育厅科研基金资助项目(2007304)
摘    要:利用分子克隆技术,通过RT-PCR反映扩增、克隆、测序含有Eco RⅠ/XhoⅠ酶切位点的MyoG片段,构建真核荧光表达载体pEGFP-N1-MyoG,并通过脂质体瞬时转染鸡成纤维细胞,对表达产物进行RT-PCR和SDS-PAGE鉴定。结果表明,经脂质体介导重组体pEGFP-N1-MyoG可成功转染鸡成纤维细胞,RT-PCR和SDS-PAGE电泳证实pEGFP-N1-MyoG可在鸡成纤维细胞中表达出MyoG蛋白。该结果为进一步研究MyoG基因的生物学作用奠定了基础。

关 键 词:MyoG  基因克隆  真核表达

Expression in chick embryo fibroblast cell of MyoG gene
ZHANG Tingting,HU Lan,WANG Hongyan,YUAN Yaqi,HAO Wenbo,YANG Xiaoyu.Expression in chick embryo fibroblast cell of MyoG gene[J].Journal of Northeast Agricultural University,2010,41(3).
Authors:ZHANG Tingting  HU Lan  WANG Hongyan  YUAN Yaqi  HAO Wenbo  YANG Xiaoyu
Institution:College of Animal Sciences;Shenyang Agricultural University;Shenyang 110161;China
Abstract:MyoG cDNA containing Eco R Ⅰ/Xho Ⅰ sites was amplified by RT-PCR, and then cloned and sequenced. Eukaryotic expression vector pEGFP-N1-MyoG was transfected into chick embryo fibroblast cells with lipidosome, and the expression protein was detected by SDS-PAGE. The result showed that MyoG gene was cloned into pEGFP-N1 successfully, and its expression at mRNA and protein level was detected with RT-PCR and SDS-PAGE. The experiment established the basis for further study on the function of MyoG gene.
Keywords:MyoG  transfection  eukaryotic expression  
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