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/ PCR T/A cloning vector for cloning PCR product by single enzyme digestion and process for preparing thereof
/ PCR T/A cloning vector for cloning PCR product by single enzyme digestion and process for preparing thereof
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机译:/ PCR T / A克隆载体,用于通过单酶消化克隆PCR产物及其制备方法
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摘要
The present invention relates to a PCR T / A cloning vector capable of cloning a polymerase chain reaction (PCR) product by a single enzyme cleavage, and a method for preparing the same. Specifically, both of the cloning vector can be achieved by a single cleavage of the restriction enzyme XcmI. A DNA fragment is prepared that forms a deoxythymine overhang at the 3'-end, and is used to readily bind to a deoxyadenine overhang located at both 3'-ends of the PCR product. And a PCR T / A cloning vector comprising a bidirectional multi-cloning site (MCS) around both 3'-terminal deoxythymine protrusions and a method for preparing the same. The DNA fragment of the present invention can be applied to an existing vector to prepare a PCR T / A cloning vector by a simple method in a short time, and the PCR T / A cloning vector thus prepared can be used for cloning PCR products as well as for re-eluting and re-closing. It facilitates cloning and can be used as a very useful tool in molecular biology research.
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机译:PCR T / A克隆载体及其制备方法技术领域本发明涉及一种能够通过单酶切割来克隆聚合酶链反应(PCR)产物的PCR T / A克隆载体及其制备方法。具体而言,两个克隆载体均可通过限制性酶XcmI的单次切割来实现。制备DNA片段,其在3'末端形成脱氧胸腺嘧啶突出端,并用于容易地结合至位于PCR产物两个3'末端的脱氧腺嘌呤突出端。以及在两个3'-末端脱氧胸腺嘧啶突出物周围包含双向多克隆位点(MCS)的PCR T / A克隆载体及其制备方法。本发明的DNA片段可以通过简单的方法在短时间内应用于现有的载体,从而制备PCR T / A克隆载体,如此制备的PCR T / A克隆载体可以用于克隆PCR产物。以及用于重新洗脱和重新闭合。它有助于克隆,可以用作分子生物学研究中非常有用的工具。
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