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作 者:王黎霞[1,2] 王彩霞[2] 徐赓[2] 安健[2]
机构地区:[1]北京农业职业技术学院畜牧兽医系,北京102442 [2]北京农学院动物科学技术系,北京102206
出 处:《动物医学进展》2009年第11期13-16,共4页Progress In Veterinary Medicine
基 金:北京市教委资助项目(KM20071002001);北京市属市管高校人才强教计划项目(PXM2007-014207-044539)
摘 要:根据pGEX-6p-1表达载体多克隆位点,设计带有限制性内切酶酶切位点的IL-2引物,RT-PCR克隆获得目的基因,连接pGEM-T载体,转化JM109感受态细胞,经蓝白斑筛选、测序和双酶切鉴定,与pGEX-6p-1表达载体连接,转化BL21感受态细胞,经双酶切和PCR鉴定,用IPTG诱导表达,通过菌体裂解、包涵体洗涤、溶解、复性、Sepharose 4B柱层析,SDS-PAGE和Western blot检测,证明表达并纯化了IL-2融合蛋白,而且纯化的IL-2融合蛋白具有促进淋巴细胞增殖的特性。A pair of primers with restriction enzyme for prokaryotic expression were designed respectively according to the gene's CDs complete sequence.The gene was amplified by RT-PCR,then cloned into pGEM-T vector and transformed into the JM109 competent cells,the plasmid of white spot was identified by PCR and sequenced.The positive plasmid was digested by the restriction enzyme.The objective gene fragment was retrieved and cloned into expressing vector pGEX-6p-1 and transformed into BL21 competent cells.The plasmid of white spot was identified by PCR and restriction enzyme of endonucleases.The fusion proteins was expressed by different inducing conditions of IPTG,and purified by Sepharose 4B chromatography.The specific band was identified by Western blot analysis.The biological activity was tested by lymphocyte proliferation test.
分 类 号:Q74[生物学—分子生物学] S852.2[农业科学—基础兽医学]
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