首页> 外国专利> CATALYTIC DNA MOLECULE SHOWING SITE-SPECIFIC ENDONUCLEASE ACTIVITY (VARIANTS), COMPOSITION CLEAVING NUCLEIC ACID, METHOD FOR CLEAVING PHOSPHOESTER BOND IN SUBSTRATE, METHOD FOR SELECTION OF CATALYTIC DNA (VARIANTS), ENZYMATIC DNA MOLECULE (VARIANTS)

CATALYTIC DNA MOLECULE SHOWING SITE-SPECIFIC ENDONUCLEASE ACTIVITY (VARIANTS), COMPOSITION CLEAVING NUCLEIC ACID, METHOD FOR CLEAVING PHOSPHOESTER BOND IN SUBSTRATE, METHOD FOR SELECTION OF CATALYTIC DNA (VARIANTS), ENZYMATIC DNA MOLECULE (VARIANTS)

机译:具有现场特定核酸酶活性的催化DNA分子(变体),裂解核酸的成分裂解,在基质中裂解磷酸酯键的方法,选择催化DNA(变体)的方法,酶DNA分子(变体)

摘要

FIELD: biochemistry, enzymology, nucleic acids. SUBSTANCE: invention relates to enzymatic nucleic acids that are able to cleave nucleic acid sequences. Sequences of enzymatic nucleic acids are given in the description. Composition cleaving nucleic acid comprises catalytic DNA. Cleavage of phosphoester bond in substrate is carried out by mixing catalytic DNA molecule with substrate comprising such bond and the following incubation of mixture. Then molecules of catalytic DNA are separated from products of catalytic reaction. Selection of catalytic DNA molecules is carried out by mixing singlestranded molecules of catalytic DNA with nucleotide-containing substrate molecules followed by exposition and separation. Invention provides preparing molecules of catalytic DNA showing substratespecific endonuclease (enzymatic) activity. EFFECT: valuable biological and biochemical properties of nucleic acid. 66 cl, 11 dwg, 3 tbl, 5 ex
机译:领域:生化,酶学,核酸。物质:本发明涉及能够切割核酸序列的酶促核酸。说明书中给出了酶促核酸的序列。切割核酸的组合物包含催化DNA。通过将催化DNA分子与包含该键的底物混合并随后孵育混合物来进行底物中磷酸酯键的切割。然后将催化性DNA分子与催化反应产物分离。催化DNA分子的选择是通过将催化DNA的单链分子与含核苷酸的底物分子混合,然后进行暴露和分离来进行的。本发明提供了制备具有底物特异性核酸内切酶(酶)活性的催化DNA分子。效果:核酸的宝贵生物学和生化特性。 66厘升,11载重吨,3汤匙,5前

著录项

  • 公开/公告号RU2220204C2

    专利类型

  • 公开/公告日2003-12-27

    原文格式PDF

  • 申请/专利权人

    申请/专利号RU19970111204

  • 发明设计人 DZHOJS DZHERALD F.;BREJKER RONALD R.;

    申请日1995-12-01

  • 分类号C12Q1/68;C12N9/22;

  • 国家 RU

  • 入库时间 2022-08-21 22:45:20

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