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作 者:张亮[1] 王宇[1] 江乐[1] 阎瑾琦[1] 王越[1] 胡明明[1] 于继云[1]
机构地区:[1]军事医学科学院基础医学研究所
出 处:《细胞与分子免疫学杂志》2010年第7期623-626,共4页Chinese Journal of Cellular and Molecular Immunology
基 金:国家高技术研究发展计划(863)资助项目(2006AA02A237;2007AA02Z451);国家自然科学基金资助项目(30772002)
摘 要:目的:构建人hCGβ真核表达载体,稳定转染入小鼠黑色素瘤B16细胞,建立稳定表达人hCGβ的小鼠黑色素瘤细胞系。方法:采用PCR方法扩增出人hCGβ全长基因的cDNA编码区序列,利用DNA重组技术将其定向插入到真核表达载体pIRES—neo中,并加入酶切位点和6×His标签,得到重组表达质粒pIRES—neo—hCGβ-(His)6。利用阳离子脂质体介导法将其稳定转染入小鼠黑色素瘤B16细胞,经G418加压筛选出阳性克隆。RT—PCR、Western blot及免疫荧光检测人hCGβ在B16细胞中的表达。结果:经限制性内切酶鉴定及序列分析,pIRES—neo—hCGβ一(His)6重组体构建正确,最终建立的表达人hCGβ基因的B16细胞系阳性率高于90%。结论:成功构建了真核表达载体plRES—neo—hCGβ-(His)6,建立的稳定转染人hCGβ小鼠黑色素瘤细胞系能够高效表达hCGβ基因。该稳定转染细胞系的建立为进一步研究人hCGβ抗肿瘤基因疫苗的功能提供了良好的实验基础,为hCGβ在肿瘤免疫治疗中的应用奠定了研究基础。AIM: To construct the eukaryotic expression vector of human hCGβ and stably transfect B16 cell line with it. METHODS: The full length of hCGβ cDNA fragment was amplified by PCR and inserted into eukaryotic expression vector plRES-neo, added the restriction enzyme position and 6 x His tag. After identification of restriction digestion and PCR, The recombinant plasmid plRES-neo-hCGβ- (His)6 was obtained. Then transfected it into BI6 cells by lipofectamine 2000. After screening culture by G418, a stably transfected cell line was established, the transcription and expression of the hCGβ gene was identified by RT-PCR, Western blot and immunofluorescence assay. RESULTS. The eukaryotic expression vector plRES-neo-hCGβ-( His)6 was successfully constructed. A stably transfected cell line was established and the expression rate of hCGβ gene was higher than 90%. CONCLUSION: The established cell line can highly express hCGβ stably, the expression of the target gene provide a solid experimental foundation for further studies on the function of the hCGβ, and which will contribute to the research of hCGβ gene in the tumor immunotherapy.
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