首页 | 本学科首页   官方微博 | 高级检索  
     

抑癌基因p16^INK4真核表达转移载体的构建
引用本文:朱长军 张利宁. 抑癌基因p16^INK4真核表达转移载体的构建[J]. 泰山医学院学报, 2000, 21(1): 4-6
作者姓名:朱长军 张利宁
作者单位:泰山医学院免疫学教研室!山东泰安271000(朱长军),山东医科大学微生物免疫学教研室!山东济南250012(张利宁,马春红,曹英林),山东省泰山疗养院!山东泰安271000(赛宁)
基金项目:卫生部科研基金资助项目!(4 13653)
摘    要:目的 构建可应用于昆虫杆状病毒表达系统的含抑癌基因p16 INK4cDNA的重组转移载体。方法 采用定向克隆方法将抑癌基因p16 INK4cDNA全长插入转移载体质粒pSXIVVI X3,并经斑点杂交 ,PCR及酶切鉴定重组质粒。结果 经三种鉴定方法证实p16 INK4cDNA片段成功地插入转移载体pSXIVVI X3。结论 重组质粒pSXIVVI X3 p16构建成功 ,为真核表达抑癌基因p16 INK4奠定了基础。

关 键 词:抑癌基因 p16^INK4 肿瘤 转移载体 真核表达

Construction of eukaryotic transfer vector of tumor suppressor gene p16~( INK4)
ZHU Chang jun ,ZHANG Li ning ,MA Chun hong ,CAO Ying lin ,SAI Ning. Construction of eukaryotic transfer vector of tumor suppressor gene p16~( INK4)[J]. Journal of Taishan Medical College, 2000, 21(1): 4-6
Authors:ZHU Chang jun   ZHANG Li ning   MA Chun hong   CAO Ying lin   SAI Ning
Affiliation:ZHU Chang jun 1,ZHANG Li ning 2,MA Chun hong 2,CAO Ying lin 2,SAI Ning 3
Abstract:Objective: To obtain the eukaryotic expression transfer vector containing the tumor suppressor gene p16 INK4 cDNA. Methods:By directional cloning method, p16 INK4 cDNA fragment was cloned into the transfer vector pSXIVVI X 3 and the recombinant plasmid DNA was identified with dot blot hybridization, PCR, and enzyme digestion. Results: p16 INK4 cDNA fragment had been cloned into the transfer vector pSXIVVI X 3 successfully. Conclusion: The recombinant plasmid pSXIVVI X 3 p16 is constructed successfully, which lays a good basis for expressing p16 INK4 gene with insect bacularvirus expression system.
Keywords:tumor suppressor gene  p16~(INK4)  insect bacularvirus expression system  transfer vector
本文献已被 CNKI 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号