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    • 5. 发明公开
    • Fractionation method for nucleotide fragments
    • FraktioniermethodefürNukleotidfragmente。
    • EP0649852A1
    • 1995-04-26
    • EP94116671.2
    • 1994-10-21
    • HITACHI, LTD.
    • Kambara, HidekiOkano, KazunoriUematsu, Chihiro
    • C07H1/06C12Q1/68
    • G01N27/44743C12Q1/6837C12Q1/6874G01N27/447C12Q2535/101C12Q2525/179C12Q2565/537C12Q2525/191
    • A fractionation method for DNA fragments according to the present invention comprises a first step of preparing a probe chip or a set of probe chips immobilizing independently a DNA probe having a first sequence part having a specific known sequence part together with a part of enzyme recognition sequence and a second sequence part composed of a combination of one to six bases adjacent to the first sequence part at 3' terminus, a second step of introducing a DNA oligomer composed of a part of enzyme recognition sequence and a sequence complementary to the known sequence part into the fragment termini of DNA fragments from restriction enzyme cleavage, and a third step of placing the probe chip or the set of probe chips in a solution containing the nucleotide fragments with the introduced DNA oligomer produced at the second step, for at least hybridization and the complementary strand extension of the DNA probe, whereby the DNA fragments are fractionated.
    • 根据本发明的DNA片段的分级方法包括制备探针芯片或一组探针芯片的第一步骤,其独立地固定有具有特定已知序列部分的第一序列部分的DNA探针以及酶识别序列的一部分 和由3'末端与第一序列部分相邻的1〜6个碱基的组合构成的第2序列部分,第2步骤,导入由部分酶识别序列构成的DNA寡聚物和与已知序列部分互补的序列 进入限制酶切割的DNA片段的片段末端,以及第三步骤,将探针片或该组探针片放置在含有第二步产生的引入的DNA寡聚物的核苷酸片段的溶液中至少杂交和 DNA探针的互补链延伸,从而分离DNA片段。