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作 者:许键[1] 李仁敬[1] 孙严[1] 杨金菊[1] 喻梅辉[1]
机构地区:[1]新疆农科院核生所
出 处:《新疆农业大学学报》1995年第3期30-34,共5页Journal of Xinjiang Agricultural University
基 金:国家自然科学基金
摘 要:本研究建立了转目的基因植物基因整台及表达的分子生物学鉴定系统,并用报告基因检测、SDS-PAGE、Dot-ELISA、PCR特异扩增、Western-Blot等方法,研究了用叶盘法经Ti质粒转化的甜瓜再生植株CMV-CP基因的整合与表达。结果表明:再生植株基因组中整合了CMV-CP基因,长度为1kb,并能有效表达。表达产物分子量为24Kd,确为CMV的外壳蛋白,其表达量占细胞总蛋白约5%。The system was established for the integration and expression assay of the purpose genes transfered into plants. Based on the techniques in this system,namely,reporter gene detection,SDS-PAGE, Dot-ELISA, PCR specific gene amplification and Western-Blot,such assay of CMV--Coat Protein (CP)gene,which had been transfered into honeymelon by Ti plaSmid using leaf-disc method,waS studied. The results showed that the Ikb CMV-CP gene did integrate with the genome of the regenerated plant. In addition,it had been ascertained that the expressed product of the gene was CMV-CP,with molecular weight of 24kd,which was produced efficiently to make up 5% of the total proteins in the gene-transfered honeymelon.
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