节点文献

人肝再生增强因子和荧光蛋白基因在绵羊成纤维细胞中的表达

ALR and EGFP gene expression in sheep fetal fibroblasts cell

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 扈会平马玉珍扈廷茂

【Author】 Hu heiping1.2,Ma yuzhen2,Hu Tingmao2 (1.Livzon(group) pharmaceuti factory zuhai 519000, 2.Faculty of life sciences,Inner Mongolia university,Huhhot 010021)

【机构】 丽珠制药厂内蒙古大学生命科学学院

【摘要】 本实验利用LipofectAMINETM介导pEGFP/ALR载体转染sFFCs,经G418筛选,10d后共形成38个单克隆细胞,细胞用于提取蛋白进行聚丙烯酰胺凝胶电泳及免疫组化检测。结果表明:3个荧光单克隆细胞,聚丙烯酰胺凝胶电泳可见与预期相符的57KD大小的融合蛋白,免疫组化检测可见ALR蛋白分布于sFFCs胞质和胞核,且细胞核含量多于细胞质。

【Abstract】 Sheep fetal fibroblasts were transfected with pEGFP-C1/ALR using LipofeetAMINETM.The transfected cells were incubated in the selected media containing 800ug/ml G418.Totally 38 clones were formed 10 days later. SDS-PAGE results indicated that there was specific 57KD protein band in the positive clons and a negative clon. Immunohistochemical analysis also indicated the expression of ALR gene were distributed in cytoplasm and nuclear, which matches the expression of GFP as well.Therefore,GFP can be used as a marker for target gene in the screening of transgenic cells and tissues.

【关键词】 人肝再生增强因子EGFP成纤维细胞表达
【Key words】 ALREGFPfetal fibroblasts cellexpression
  • 【文献出处】 北方药学 ,Journal of North Pharmacy , 编辑部邮箱 ,2007年06期
  • 【分类号】R96
  • 【下载频次】11
节点文献中: