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卡介苗ERP基因置换型打靶载体的构建
引用本文:吴芳,张万江,曹旭东,黄春,吴江东.卡介苗ERP基因置换型打靶载体的构建[J].农垦医学,2005,27(5):332-334.
作者姓名:吴芳  张万江  曹旭东  黄春  吴江东
作者单位:石河子大学新疆地方与民族高发病重点实验室,新疆,石河子,832002
摘    要:目的:构建ERP基因打靶载体。方法:卡介前菌体外培养,扩增ERP基因两侧序列.连接载体与目的片段.筛选阳性克降并鉴定。结果:PCR扩增捕入片段大小与预期相符.鉴定证实PCR产物及插入片段为所需目的基因片段。结论:成功构建了用于卡介苗菌基因打靶的置换型载体,为今后构建ERP基因敲除株的卡介苗突变株的研究奠定基础。

关 键 词:基因敲除  ERP基因  卡介苗菌

Construction of the gene targeting vector of ERP gene in BCG
Wu Fang,Zhang Wanjiang,Cao Xudong,Huang Chun,Wu Jiangdong.Construction of the gene targeting vector of ERP gene in BCG[J].Agricultural Reclamation Medicine,2005,27(5):332-334.
Authors:Wu Fang  Zhang Wanjiang  Cao Xudong  Huang Chun  Wu Jiangdong
Institution:Laboratory of Xinjiang Endemic and Ethnic Diseases,Shihezi University,Shihezi,Xinjiang 832002,China
Abstract:Objective: In order to knockout erp gene in BCG, the sideward gene of erp was amplified and gene targeting vector was constructed. Methods: Culturing the BCG in vitro, extracting the genome DNA, amplifying the targeted gene with PCR, constructing the gene targeting vector and identitying it. Results: The fragment was amplified successfully. The replacement vector with deleted erp gene was constructed. Conclusion: Constructing successfully the replacement vector which is used to the gene knockout in BCG.
Keywords:Gene knockout  erp gone  BCG
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