|本期目录/Table of Contents|

[1]胡徐庞a,李伟a,曹跃芬b,等. 真核表达HsamiR1基因及其检测方法的建立[J].浙江理工大学学报,2011,28(05):783-788.
 HU Xu panga,LI Weia,CAO Yue fenb,et al. Eukaryotic Expression of HsamiR1 Gene and Establishment of Its Detection Method[J].Journal of Zhejiang Sci-Tech University,2011,28(05):783-788.
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 真核表达HsamiR1基因及其检测方法的建立()
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浙江理工大学学报[ISSN:1673-3851/CN:33-1338/TS]

卷:
第28卷
期数:
2011年05期
页码:
783-788
栏目:
(自科)生物与生命科学
出版日期:
2011-10-30

文章信息/Info

Title:
 Eukaryotic Expression of HsamiR1 Gene and Establishment of Its Detection Method
文章编号:
16733851 (2011) 05\|078306
作者:
胡徐庞a 李伟a 曹跃芬b 张璇a 黄青红a徐科a 杨耿兵a 魏旭斌a 钱程a 刘立a
 浙江理工大学生命科学学院, a. 新元医药研究所; b. 生物工程研究所, 杭州 310018
Author(s):
 HU Xupanga LI Weia CAO Yuefenb ZHANG Xuana HUANG Qinghonga XU Kea YANG Gengbina WEI Xubina QIAN Chenga LIU Lia
 Zhejiang SciTech University, a. Xinyuan Institute of Medicine and Biotechnology; b. Institute of Bioengineering, Hangzhou 310018, China
关键词:
 HsamiR1载体 Taqman探针检测 pcDNAHsamiR1 pEGFPC1CM1
分类号:
Q786
文献标志码:
A
摘要:
    获得HsamiR1的方法主要由人工合成,需耗费很高的成本与时间。文章通过将HsamiR1前体部分连接至pcDNA3.0,可实现HsamiR1基因的高表达。构建含有HsamiR1基因表达前体的表达载体pcDNAHsamiR1和含有与HsamiR1基因完全互补序列的检测载体pEGFPC1CM1。通过共转染pcDNAHsamiR1和pEGFPC1CM1检测HsamiR1基因的表达,并采用Taqman探针法定量检测HsamiR1基因表达水平,成功构建了可高效表达HsamiR1基因的真核生物质粒pcDNAHsamiR1,并首次建立起HsamiR1基因的检测系统pEGFPC1CM1,该检测系统的建立将为今后HsamiR1在肿瘤细胞中的研究提供准确、快捷的检测方法。

参考文献/References:

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备注/Memo

备注/Memo:
 收稿日期: 2010-12-20
基金项目: 国家重点基础发展计划资助项目(973)(2010CB529406)
作者简介: 胡徐庞(1983-),男,浙江金华人,硕士研究生,从事肿瘤基因治疗研究。
通讯作者: 刘立,电子邮箱:liuli7001@yahoo.com.cn
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