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 |
代理机构 |
|
代理人 |
|
主权项 |
|
地址 |
|