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甲胎蛋白增强子调控的小干扰RNA质粒载体的构建

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甲胎蛋白增强子调控的小干扰RNA质粒载体的构建

贺军;王艳;姜浩;唐静波;李珍发;张阳德

【期刊名称】《中华实验外科杂志》 【年(卷),期】2009(026)008

【摘要】目的 构建AFP增强子调控的小干扰RNA质粒载体.方法 从HePG2细胞中提取AFP基因.采用定向克隆的方法,构建质粒pGenesil-AFP.pGenesil-AFP质粒DNA扩增、提取后转化到DH5感受态细胞.针对目的 基因Survivin的序列,构建pGenesil-AFP-shRNA.结果 pGen-esil-AFP-shRNA质粒经XbaI和Hind Ⅲ双酶切鉴定,获得一856 bp大小和4506 bp大小的片段,通过基因测序分析,证明质粒载体构建正确,用紫外分光光度计测得质粒的浓度为1.3 g/L,A值为1.94,说明制备的质粒纯度较高.结论 成功构建AFP增强子调控的Survivin shRNA融合质粒.%Objective To construct an AFP enhancer-regulated siRNA expression plasmid vector.Methods The AFP gene was extracted from HePG2 cells, constructing plasmid PGenesil-AFP by orientation cloned.After DNA extraction and amplification, Plasrnid pGenesil-AFP was transformed into competent cell of DHS.Constructing plasmid vector pGenesil-AFP-shRNA to aim at the target gone sruvivin' s sequence.Results After p]asmid pGenesil-AFP-shRNA evaluated by gene sequencing analysis and enzyme cutting with both XbaⅠ and Hind Ⅲ, obtain a fragment of 856 bp and a fragment of 4506 bp.It is prove that Plasmid can be successfully constructed.Measured by ultraviolet spectrophotometer, the concentration of plasmid is 1.3 g/L and A value

甲胎蛋白增强子调控的小干扰RNA质粒载体的构建

甲胎蛋白增强子调控的小干扰RNA质粒载体的构建贺军;王艳;姜浩;唐静波;李珍发;张阳德【期刊名称】《中华实验外科杂志》【年(卷),期】2009(026)008【摘要】目的构建AFP增强子调控的小干扰RNA质粒载体.方法从HePG2细胞中提取AFP基因.采用定向克隆的方法,构建质粒pGenesil-AFP.pGenesil-A
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