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METHOD FOR DETECTING NONSENSE MUTATIONS AND FRAMESHIFT MUTATIONS

机译:检测无意义变异和框架变异的方法

摘要

A method for conveniently detecting nonsense mutations and frameshiftmutations, which is applicable even to large-sized test DNAs. This methodcomprises inserting, into a vector containing a promoter, an initiation codonlocated downstream the promoter and a reporter gene located downstream theinitiation codon which is a structural gene under the regulation by thepromoter and a fused polypeptide consisting of the polypeptide encoded bywhich and another polypeptide bonded to the N-terminus of the formerpolypeptide can be detected based on the function of the polypeptide encodedby the structural gene, a test nucleic acid fragment which makes the readingframe of the reporter gene to match the above-mentioned initiation codon whenit is a normal type one to a site downstream the initiation codon but upstreamthe reporter gene; expressing the test nucleic acid fragment in therecombinant vector thus obtained and the reporter gene downstream the same inhost cells; and thus examining whether or not a fused polypeptide having thefunction of the polypeptide encoded by the reporter gene is produced.
机译:一种方便地检测废话突变和移码的方法突变,甚至适用于大型测试DNA。这个方法包括将起始密码子插入含有启动子的载体中位于启动子的下游和位于其下游的报告基因起始密码子是在启动子和融合多肽,由其中一个和另一个多肽与前者的N端键合可根据编码的多肽的功能检测多肽通过结构基因,一个测试核酸片段报道基因的框架与上述起始密码子匹配这是一种正常类型,位于起始密码子下游但上游的位点报告基因;在其中表达测试核酸片段由此获得的重组载体及其下游的报告基因宿主细胞;从而检查是否具有产生了由报告基因编码的多肽的功能。

著录项

  • 公开/公告号CA2240018A1

    专利类型

  • 公开/公告日1998-04-16

    原文格式PDF

  • 申请/专利权人 SRL INC.;

    申请/专利号CA19972240018

  • 申请日1997-10-07

  • 分类号C12Q1/68;

  • 国家 CA

  • 入库时间 2022-08-22 02:53:59

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