发明名称 LINEAR AMPLIFICATION METHOD FOR TRACE DNA FRAGMENT
摘要 <p>The amplification by an LM-PCR method has such a problem that amplification accuracy is not satisfactory although amplification sensitivity is high, and the amplification by a T7-IVT method has such a problem that amplification sensitivity is not satisfactory although amplification accuracy is high. The present invention provides a nucleic acid amplification method whereby it becomes possible to solve the problems of these conventional methods. A nucleic acid amplification method comprising the following step (a) and/or step (b): (a) a step of carrying out an enzymatic reaction of a terminal nucleotide transferase in the presence of DNA which cannot be added with a base at the 3'-terminal thereof with the terminal nucleotide transferase; and (b) a step of carrying out the enzymatic reaction of a Klenow enzyme in the co-presence of a poly(A-T7) oligo-DNA primer and the Klenow enzyme and in the presence of DNA that cannot undergo the formation of any double strand in a T7 region of the poly(A-T7) oligo-DNA primer.</p>
申请公布号 WO2013047677(A1) 申请公布日期 2013.04.04
申请号 WO2012JP74927 申请日期 2012.09.27
申请人 PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY 发明人 TANIGUCHI, HIDEKI;UENO, YASUHARU
分类号 C12N15/09;C12N9/10;C12N9/96;C12P19/34;C12Q1/68 主分类号 C12N15/09
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