首页 | 本学科首页   官方微博 | 高级检索  
     

nm23H1正反义表达载体的构建
引用本文:金嗣松,潘星华,王元和,胡以平,傅继梁. nm23H1正反义表达载体的构建[J]. 第二军医大学学报, 1999, 20(6): 350-352
作者姓名:金嗣松  潘星华  王元和  胡以平  傅继梁
作者单位:1. 第二军医大学长征医院普通外科
2. 第二军医大学基础医学部生物学教研室,上海,200433
摘    要:目的;构建nm23H1正反义表达载体pc3AN和pc3AM。方法:将nm23H1基因正,反向插入质粒pcDNA3和pRC/CMV,并转染肝癌细胞SMMC7721。结果:转染正义表达载体后nm23H1mRNA和蛋白表达水平增加,转染反义表达载体后nm23H1mRNA和蛋白表达水平降低。结论:构建的载体能在肝癌细胞内有效表达。

关 键 词:基因  表达载体  肝肿瘤

Construction of expression vector of sense and antisense nm23H1
Jin Sisong,Pan Xinghua,Wang Yuanhe,Hu Yiping,Fu Jiliang. Construction of expression vector of sense and antisense nm23H1[J]. Former Academic Journal of Second Military Medical University, 1999, 20(6): 350-352
Authors:Jin Sisong  Pan Xinghua  Wang Yuanhe  Hu Yiping  Fu Jiliang
Abstract:Objective: To construct expression vector of sense and antisense nm23H1: pc3AN and pc3AM. Methods: nm23H1 gene was inserted into plasmid pcDNA3 and pRC/CMV in proper sequence and in reverse sequence, the production of above action was used to transfect liver cancer cell SMMC7721. Results: The level of mRNA and protein of nm23H1 was high when transfected with sense vector, and was low when transfected with antisense vector. Conclusion: The constructed vectors can highly express in liver cancer cell.
Keywords:nm23H1
本文献已被 CNKI 维普 万方数据 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