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filingDate 2002-03-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a1af2873d34b149fbc18044506ea9e25
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publicationDate 2002-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2002355081-A
titleOfInvention Method for producing self-assembly using oligonucleotide and method for detecting gene
abstract (57) [Summary] [Problem] To provide a method for producing a self-assembly with reduced reaction time, expansion of the optimal reaction temperature range, improved operability and applicability, and a simple method for detecting a gene using the method. I do. SOLUTION: For the formation of a plurality of pairs of dimers, the base region is composed of three regions of 3 'side, center and 5' side and the central region is complementary to each other and the 3 'and 5' side regions are non-complementary to each other. Using a probe and a plurality of pairs of cross-linking probes each comprising a 3′-side and a 5′-side region and comprising a non-complementary base sequence in the 3′-side and 5′-side regions, the cross-linking probe is subjected to the dimer formation. The dimer formed from the probe for use was formed into a base sequence capable of crosslinking, and the probe was hybridized so that the oligonucleotides self-assembled to form a double-stranded regular higher-order structure.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2013172305-A1
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