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IMPROVED URACIL-EXCISION BASED MOLECULAR CLONING

机译:改进的基于尿嘧啶的分子克隆

摘要

The invention provides an improvement to a uracil-specific excision reagent (USER™) based cloning technique comprising generating a single-stranded extension on a polynucleotide molecule, the single-stranded extension having a desired length and sequence composition, comprising: (a) introducing a cassette into a polynucleotide molecule at a predetermined location; (b) cleaving the polynucleotide molecule with a nicking endonuclease specific for a nicking site in the cassette and with a restriction endonuclease specific for a restriction site in the cassette; and (c) dissociating the cleaved polynucleotide molecule between the nicking site and the restriction site to generate the single-strand extension with the desired length and sequence composition; wherein said improvement to said USER™ based cloning technique comprises using a proof-reading polymerase to generate said polynucleotide molecule. Also provided is a deoxyuridine-excision based method of fusing duplex nucleic acid sequence to form a fused duplex product referred to herein as 'USER™ fusion'. The invention further provides related materials and methods.
机译:本发明提供了基于尿嘧啶特异性切除试剂(USER TM)的克隆技术的改进,其包括在多核苷酸分子上产生单链延伸,该单链延伸具有期望的长度和序列组成,包括:(a)引入在预定位置将盒放入多核苷酸分子中; (b)用特异于盒中切口位点的切口内切核酸酶和特异于盒中限制位点的限制性核酸内切酶切割多核苷酸分子; (c)使切割的多核苷酸分子在切口位点和限制位点之间解离,以产生具有所需长度和序列组成的单链延伸;其中对所述基于USER TM的克隆技术的所述改进包括使用校对聚合酶产生所述多核苷酸分子。还提供了基于脱氧尿苷切除的融合双链体核酸序列以形成融合的双链体产物的方法,在本文中称为“ USER TM融合体”。本发明进一步提供了相关的材料和方法。

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