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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c6baa9faf17bb2a79be845fd9d61b449
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-1247
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-92
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-12
filingDate 2002-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a8bd464eff1324669ce32a94de033131
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publicationDate 2004-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1403364-A1
titleOfInvention Mutant rna polymerases
abstract It is intended to provide novel mutant RNA polymerases enabling a transcriptional sequencing method whereby a high SN ratio can be achieved in sequence analysis with the use of capillary and longer and more accurate base sequencial data can be obtained by a single reaction. More specifically, a mutant RNA polymerase derived from a wild type RNA polymerase by substitution of at least one amino acid and deletion of at least one amino acid, or a mutant RNA polymerase derived from a wild type RNA polymerase by deletion of at least one amino acid, wherein the above-described substitution and/or deletion of amino acid(s) have been performed so that the resultant mutant RNA polymerase has an enhanced ability to incorporate 3'-deoxynucleotide as a substrate compared with the wild type RNA polymerase corresponding thereto.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9062292-B2
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priorityDate 2001-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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