会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 1. 发明授权
    • Method of double stranded DNA synthesis
    • 双链DNA合成方法
    • US5681726A
    • 1997-10-28
    • US116049
    • 1993-09-02
    • William David HuseConnie Jo Hansen
    • William David HuseConnie Jo Hansen
    • C12N15/10C12P19/34
    • C12N15/1096
    • The present invention provides an improved method for the synthesis of double stranded DNA, particularly complementary DNA for the construction of directional complementary DNA libraries. The method comprises synthesizing a first strand of DNA complementary to a selected RNA or DNA template by contacting with the template a linker/primer comprising a selected restriction site, a suitable RNA or DNA dependent DNA polymerase, and substrates comprising a deoxyribonucleotide triphosphate analog. The linker/primer and deoxyribonucleotide triphosphate analog are selected such that incorporation of the nucleotide analog in the first strand substantially protects the double stranded DNA from cleavage, under conditions sufficient to cleave or substantially cleave the linker/primer, at the selected restriction site.
    • 本发明提供了用于合成双链DNA,特别是用于构建定向互补DNA文库的互补DNA的改进方法。 该方法包括通过与模板接触来合成与所选择的RNA或DNA模板互补的第一链,包含选定的限制性位点,合适的RNA或DNA依赖性DNA聚合酶的接头/引物,以及包含脱氧核糖核苷酸三磷酸类似物的底物。 选择接头/引物和脱氧核苷酸三磷酸类似物,使得在所选择的限制性位点处,在足以切割或基本上切割接头/引物的条件下,在第一链中的核苷酸类似物的引入基本上保护双链DNA不被切割。
    • 10. 发明授权
    • Method of double stranded DNA synthesis
    • 双链DNA合成方法
    • US6143531A
    • 2000-11-07
    • US899029
    • 1997-07-22
    • William David HuseConnie Jo Hansen
    • William David HuseConnie Jo Hansen
    • C12N15/10C12P19/34C07H21/04
    • C12N15/1096
    • The present invention provides an improved method for the synthesis of double stranded DNA, particularly complementary DNA for the construction of directional complementary DNA libraries. The method comprises synthesizing a first strand of DNA complementary to a selected RNA or DNA template by contacting with the template a linker/primer comprising a selected restriction site, a suitable RNA or DNA dependent DNA polymerase, and substrates comprising a deoxyribonucleotide triphosphate analog. The linker/primer and deoxyribonucleotide triphosphate analog are selected such that incorporation of the nucleotide analog in the first strand substantially protects the double stranded DNA from cleavage, under conditions sufficient to cleave or substantially cleave the linker/primer, at the selected restriction site.
    • 本发明提供了用于合成双链DNA,特别是用于构建定向互补DNA文库的互补DNA的改进方法。 该方法包括通过与模板接触来合成与所选择的RNA或DNA模板互补的第一链,包含选定的限制性位点,合适的RNA或DNA依赖性DNA聚合酶的接头/引物,以及包含脱氧核糖核苷酸三磷酸类似物的底物。 选择接头/引物和脱氧核苷酸三磷酸类似物,使得在所选择的限制性位点处,在足以切割或基本上切割接头/引物的条件下,在第一链中的核苷酸类似物的引入基本上保护双链DNA不被切割。