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人4-1BBL基因重组腺病毒载体的构建及其在HEK293细胞的表达
引用本文:杨明花,王帅,田昕,王扬,隋承光. 人4-1BBL基因重组腺病毒载体的构建及其在HEK293细胞的表达[J]. 解剖科学进展, 2011, 17(5): 445-449
作者姓名:杨明花  王帅  田昕  王扬  隋承光
作者单位:中国医科大学附属第一医院肿瘤研究所,辽宁,沈阳,110001
基金项目:辽宁省科技厅科学技术计划项目
摘    要:目的 体外构建含有人4-IBBL基因的重组腺病毒载体,并检测其在HEK293细胞中的表达.方法 设计一对含有Sfil酶切位点的4-1BBL因上下游引物,以质粒pCR4-TOP0-4-1BBL为模板,通过PCR扩增获得4-1BBL基因全序列.片段回收后经酶切处理,连接到穿梭质粒pShuttle-CMV-EGFP上,获得重...

关 键 词:4-1BBL  腺病毒  基因表达  共刺激分子

Construction and expression of human 4-1BBL recombinant adenovirus vector in HEK293 cells
YANG Ming-hua,WANG Shuai,TIAN Xin,WANG Yang,SUI Cheng-guang. Construction and expression of human 4-1BBL recombinant adenovirus vector in HEK293 cells[J]. Progress of Anatomical Sciences, 2011, 17(5): 445-449
Authors:YANG Ming-hua  WANG Shuai  TIAN Xin  WANG Yang  SUI Cheng-guang
Affiliation:YANG Ming-hua,WANG Shuai,TIAN Xin,WANG Yang,SUI Cheng-guang* (Cancer Research Institute,First Affiliated Hospital,China Medical University,Shenyang 110001 China)
Abstract:Objective To construct the recombinant adenovirus vector contained human 4-1BBL gene and to check the target gene expression in HEK293 cells. Methods Primer containing SfiI was designed and full length 4-1BBL cDNA was obtained from the pCR4-TOPO-4-1BBL plasmid by PCR, the PCR product was digested with restrictive endonucleases SfiI, then inserted directionally into pShuttle-CMV-EGFP. The plasmid of pShuttle-EGFP-4-1BBL was lined with SfiiI, the fragment containing 4-1BBL was reclaimed and then transfected i...
Keywords:4-1BBL  adenovirus  gene expression  costimulating molecule  
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