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METHOD FOR CELL-FREE TRANSCRIPTION OF DNA MATRIX, METHOD FOR IDENTIFYING TESTING SUBSTANCE, DNA MATRIX

机译:DNA基质的无细胞转录方法,鉴定测试物质的方法,DNA基质

摘要

FIELD: biotechnology, molecular biology, genetics.;SUBSTANCE: invention can be used for in vitro analysis in transcription of viral and cellular genes. Cell-free transcription of DNA matrix in vitro is carried out using enriched extract from cellular nuclei and marked nucleotide and marked transcript is determined. DNA matrix comprises unique restriction sites for site-specific restriction endonucleases: Pst I, Eco RI, Sac I, Kpu I, Sac II, Bam HI, Swa I, part of plasmid pUC19, five sites for binding yeast protein Ga14, "TATA"-block of human receptor of T cells Vβ 8.1 between restriction sites Sac II and Bam HI, initiating site of adenovirus of the main later promoter between restriction sites Bam HI and Swa I and G-free sequence with length about 800 nucleotides. Invention provides carrying out the detection of specific transcript in automatic regimen.;EFFECT: improved method for transcription.;50 cl, 3 dwg, 1 tbl, 7 ex
机译:领域:生物技术,分子生物学,遗传学;物质:本发明可以用于病毒和细胞基因转录的体外分析。使用来自细胞核的富集的提取物和标记的核苷酸进行体外DNA基质的无细胞转录,并确定标记的转录本。 DNA基质包含针对位点特异性限制性核酸内切酶的独特限制性位点:Pst I,Eco RI,Sac I,Kpu I,Sac II,Bam HI,Swa I,质粒pUC19的一部分,五个结合酵母蛋白Ga14的位点,“ TATA”受体对T细胞V&β的阻断8.1在限制性酶切位点Sac II和Bam HI之间,主要后期启动子的腺病毒的起始位点在限制性酶切位点Bam HI和Swa I之间,长度为约800个核苷酸,不含G。本发明提供了以自动方案进行特异性转录物的检测。效果:改进的转录方法; 50 cl,3 dwg,1 tbl,7 ex

著录项

  • 公开/公告号RU2235787C2

    专利类型

  • 公开/公告日2004-09-10

    原文格式PDF

  • 申请/专利权人

    申请/专利号RU19980104504

  • 申请日1998-03-11

  • 分类号C12Q1/68;C12N15/63;

  • 国家 RU

  • 入库时间 2022-08-21 22:44:54

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