http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1490514-A4

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6dd45aa981988e937877aa9ed1069370
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6804
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
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filingDate 2003-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_349ca160053e0487c2cdd0621d0aec36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fe51d0c9fd9c631fdf46f74a4a706400
publicationDate 2008-12-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1490514-A4
titleOfInvention THROUGH ISOTHERME SINGLE PRIMER NUCLEIC ACID AMPLIFICATION IMPROVED DETECTION AND QUANTIFICATION OF ANALYTES
abstract The present invention provides novel methods of indirect analyte detection and quantification through amplification of oligonucleotide template attached to binding partners for analytes by nucleic acid amplification utilizing isothermal, single primer linear nucleic acid amplification methods. Methods of binding of binding partner that is attached to an oligonucleotide template to analyte, then amplifying at least a portion of the oligonucleotide template using a composite primer, primer extension, strand displacement, and optionally a termination sequence, are provided. Methods for amplifying sense RNA using a composite primer, primer extension, strand displacement, optionally template switching, a propromoter oligonucleotide and transcription are also provided. Methods for detecting and quantifying amplification products are also provided. The invention further provides compositions and kits for practicing said methods.
priorityDate 2002-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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