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PLASMID-TYPE VECTOR, METHOD FOR DETECTING GENE PROMOTER ACTIVITY AND ASSAY KIT

机译:质粒型矢量,检测基因启动子活性和检测试剂盒的方法

摘要

PROBLEM TO BE SOLVED: To detect activity of a gene promoter in high sensitivity.SOLUTION: The plasmid-type vector 1 has a gene promoter 10. A reporter gene 21, an internal ribosome entry site (IRES) 23, a replication initiation protein gene 25, and a transcription termination signal sequence 27 are arranged at the downstream of the gene promoter 10. The reporter gene 21 encodes a reporter protein for visualizing activity of the gene promoter 10. The replication initiation protein gene 25 encodes the replication initiation protein. The IRES 23 is arranged between the reporter gene 21 and the replication initiation protein gene 25. The transcription termination signal sequence 27 encodes a signal for terminating transcription of the reporter gene 21 and the replication initiation protein gene 25. The plasmid-type vector 1 has a replication initiation sequence 30. The replication initiation sequence 30 is recognized by the replication initiation protein.
机译:解决的问题:以高灵敏度检测基因启动子的活性。解决方案:质粒型载体1具有基因启动子10。报告基因21,内部核糖体进入位点(IRES)23,复制起始蛋白基因如图25所示,在基因启动子10的下游配置有转录终止信号序列27,在基因启动子10的下游配置有转录终止信号序列。报告基因21编码用于使基因启动子10的活性可视化的报告蛋白。复制起始蛋白基因25编码复制起始蛋白。 IRES 23布置在报告基因21和复制起始蛋白基因25之间。转录终止信号序列27编码用于终止报告基因21和复制起始蛋白基因25转录的信号。质粒型载体1具有复制起始序列30。复制起始序列30被复制起始蛋白识别。

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