摘要
目的:克隆Motilin和ghrelin基因,构建表达Motilin的pDsRed-Express-motilin载体和表达ghrelin的pEGFP-ghrelin载体,并检测它们能否在真核细胞中表达及表达量的变化。方法:用RT-PCR方法分别从猪小肠和胃的cDNA上扩Motilin和ghrelin基因片段,并分别克隆到pDsRed-Express-N1载体和pEGFP-N1载体上,用脂质体法转染RIBS2细胞系(来自于肾),并用半定量RT-PCR和荧光成像法检测目的基因的表达。结果:构建了表达Motilin的pDsRed-Express-motilin和表达ghrelin基因的pEGFP-ghrelin载体,并能在真核细胞中超表达目的基因,为进一步相关研究提供了实验基础。
Aim: clone big motilin and ghrelin gene, construct recombinant pDsRed-expree-motilin and pEGFP-ghrelin vector and their expressions in vitro. Method: motilin and ghrelin genes were amplified by PCR and were cloned to pDsRed-Express-N1 and pEGFP-N1, respectively. Then the resultant pDsRed -Express-Motilin and pEGFP-ghrelin were co-transferred into RIBS2 ceils with lipd2000. Result: construction combinations of pDsRed-Express-motilin and EGFP-ghrelin vectors are successful and their expressions are highly efficient in RIBS2 cells.
出处
《江西科技师范学院学报》
2006年第6期103-106,共4页
Journal of Nanchang Vocational & Technical Techers' College