发明名称
摘要 PROBLEM TO BE SOLVED: To provide both a method for preparing a self-assembly having a shortened reactional time, an extended optimum reactional temperature region and an improved operating efficiency and applicability and a simple method for detecting a gene utilizing the method. SOLUTION: This method for preparing the self-assembly comprises using a plurality of pairs of probes for forming a dimer in which each of a pair of oligonucleotides is divided into three regions of a 3'-terminal region, the central region and a 5'-terminal region and base sequences in the central region of the oligonucleotides are made mutually complementary while base sequences in the 3'-terminal region and the 5'-terminal region are made mutually noncomplementary and a plurality of pairs of cross- linking probes in which each of a pair of oligonucleotides is divided into two regions of a 3'-terminal region and a 5'-terminal region and base sequences in the 3'-terminal region and the 5'-terminal region are made mutually noncomplementary, converting the cross-linking probes into the base sequences capable of cross-linking the dimer formed from the probes for forming the dimer and thereby hybridizing the probes. As a result, oligonucleotides are self-assembled and a double-stranded regular high-order structure is formed.
申请公布号 JP4121757(B2) 申请公布日期 2008.07.23
申请号 JP20020074553 申请日期 2002.03.18
申请人 发明人
分类号 C12N15/09;G01N21/64;C12Q1/25;C12Q1/68;G01N21/33;G01N33/53;G01N33/566;G01N33/58 主分类号 C12N15/09
代理机构 代理人
主权项
地址