发明名称 DNA fragment detection method, DNA fragment detection kit and the use thereof
摘要 The disclosure claims a cleaved Deoxyribonucleic acid (DNA) detection method, a DNA fragment detection kit and use thereof. Wherein, the method includes the steps of: designing primers according to a test site or a test region of the DNA fragment; cyclizing the DNA fragment to obtain acyclized DNA; implementing Polymerase Chain Reaction (PCR) amplification for the cyclized DNA by using the primers; and detecting the PCR amplification product. In the disclosure, by cyclizing the DNA fragment, the amplification can be implemented even if only one PCR primer can match with a template, thus, the adaption range and effective template amount of the primer amplification can be greatly increased, and the detection sensitivity of the DNA fragment can be greatly improved.
申请公布号 US9540687(B2) 申请公布日期 2017.01.10
申请号 US201214347113 申请日期 2012.07.11
申请人 BERRY GENOMICS CO., LTD. 发明人 Zhang Jianguang;Zhou Zhongchun;Zhou Daixing;Xu Genming;Gao Yang;Tian Feng
分类号 C12Q1/68 主分类号 C12Q1/68
代理机构 Whiteford, Taylor & Preston, LLP 代理人 Whiteford, Taylor & Preston, LLP ;Davis Peter J.
主权项 1. A DNA fragment detection method, comprising the steps of: designing primers based on a test site adjacent sequence or a test region adjacent sequence of a DNA fragment, wherein the primers are a primer pair comprising of adjacent primers which extend backwards and the primers of the primer pair which extend backwards are all located on the 5′ end 3′ end of the test site or the test region of the DNA fragment; cyclizing the DNA fragment to obtain a cyclized DNA; implementing PCR amplification for the cyclized DNA by using the primers; and detecting a product of the PCR amplification, wherein the DNA fragment refers to a short fragment DNA which is formed by natural random fragmentation of biological genomic DNA, and has a length of 20 bp to 2000 bp.
地址 Beijing CN