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A method for the production of dna - probes for dna - sections with repetitive sequences

机译:具有重复序列的dna-区段的dna-探针的生产方法。

摘要

A method for the production of dna - probes with single strand dna - - oligomers of a repetitive sequence motif,characterized byProviding the single strand - dna - oligomers of the repetitive sequence motif as abnormal,Adding to the abnormal complementary oligomers as against sense strand,Can hybridize of sense - and to sense strand,Adding a first primer, consisting of a first primer sequence and oligomers of the repetitive sequence motif, wherein the first primer sequence is not connected to the repetitive sequence motif is identical, and adding a second primer consisting of a second primer sequence and the to the abnormal complementary oligomers of the repetitive sequence motif, wherein the second primer sequence is not connected to the repetitive sequence motif is identical,The primers hybridize,The addition of nucleotides, of a klenow - fragment and a ligase and allowed to react,Removal of single-stranded dna and dna with a length less than 100 nucleotides,Amplification of the purified dna by means of pcr andMarking of the pcr - products with a reporter molecule.
机译:一种具有重复序列基序的单链dna-寡聚体的dna-探针的生产方法,其特征在于,将所述单链-dna-重复序列基序的寡聚体提供为异常,除了针对有义链的异常互补寡聚体之外,可以杂交有义链和有义链,添加由第一引物序列和重复序列基序的寡聚物组成的第一引物,其中第一引物序列未连接至重复序列基序是相同的,并添加第二引物由第二个引物序列和重复序列基序的异常互补寡聚体组成,其中第二个引物序列未与重复序列基序连接,是相同的,这些引物与klenow片段杂交,添加核苷酸连接酶并使其反应,去除单链dna和长度小于100个核苷酸的dna,纯化嘌呤通过pcr进行dna标记和pcr标记-具有报告分子的产品。

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