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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2521-319
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6834
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 2008-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_627e50c01e5dfc8db1c8511ef8995d3e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_854b11c535caba3bcab12f278f15ee1f
publicationDate 2008-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20080078615-A
titleOfInvention Methods, compositions and kits for increasing the hybridization efficiency or specificity of a PNA probe and target nucleic acid immobilized on a support
abstract In the present invention, a target nucleic acid is fragmented by using a nuclease in a hybridization reaction of a PNA (Peptide Nucleic Acid) probe and a target nucleic acid immobilized on a support, or the size of the target nucleic acid is reduced or mismatched with the PNA probe. A method, composition and kit for increasing the hybridization efficiency or specificity between a target nucleic acid and a PNA probe immobilized on a support, comprising selectively cleaving a mismatched target nucleic acid. According to the present invention, it is possible to easily distinguish single nucleotide polymorphism (SNP) by increasing the sensitivity and specificity of the hybridization reaction in the PNA chip, and to analyze long target nucleic acids without undergoing complex amplification and pretreatment. In addition, multiple SNPs or mutations in long target nucleic acids can be detected by one target nucleic acid amplification.
priorityDate 2007-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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