http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5616478-A

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Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6834
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6848
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P19-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 1992-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1997-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a5aaf90aa99f5fc9b29dd1c47ff0cc9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee939a7ac2b5e23dbc1ba713624c4e8f
publicationDate 1997-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5616478-A
titleOfInvention Method for amplification of nucleic acids in solid media
abstract Amplification and/or expression of nucleic acids is carried out in a medium immobilized by using an organic and/or inorganic solid matrix penetrating the medium and having a porous, fibrous, reticulated, coiled, capillary, lamellar or folded texture and which includes the components of a cell-free enzyme system of exponential amplification of nucleic acids and/or components of a cell-free enzyme system of nucleic acid expression. In this medium, the progeny of each molecule (clone) and the expression products remain in the same zone of the reaction volume where the matrix molecule was initially located. The method permits cloning of nucleic acids in vitro as well as detection of solitary nuleic acid molecules in the sample studied.
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