http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2009087858-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9e8f9e7a1094964e5ce47ad57c20018d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6046d8af2c5981f5a981b9b0ec25ef45
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6851
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6818
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 2008-12-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_40dd366a1f1e601498feb728eb406c93
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3cf3da9b2b61532049d9f00e84fac842
publicationDate 2009-04-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2009087858-A1
titleOfInvention Two-color Real-time/End-point Quantitation of MicroRNAs (miRNAs)
abstract The present invention is directed to methods, reagents, kits, and compositions for detecting target polynucleotide sequences, especially small target polynucleotides such as miRNAs, between two samples. A pair of linker probes can be employed in two different reactions to query a particular species of target polynucleotide. A pair of detector probes, a single forward primer specific for the target polynucleotide, and a reverse primer can be employed in an amplification reaction to query the difference in expression level of the target polynucleotide between the two samples. In some embodiments a plurality of small miRNAs are queried with a plurality of linker probes. The plurality of queried miRNAs can then be decoded in a plurality of amplification reactions.
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priorityDate 2004-09-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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