http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2209906-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e41651508566f0385833e1ba14a21ffd
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-045
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-42
filingDate 2008-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5391940ba2bf2010f898ce67e154a640
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_32f09bcfc66b15f5336cfe2c49e1a801
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7123ac0195e4d22f83c381ef04f84a4a
publicationDate 2010-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2209906-A2
titleOfInvention Novel plating media
abstract Plating media contains enzyme substrates (ES) used to detect enzyme activity associated with a target organism and that include a binding motif (BM) that serves to bind detectable enzymes (DE) (also called marker enzymes in this disclosure). A signalogenic substructure (SG) produces detectable signals and an enzyme labile group (ELG) is labile to the action of a marker enzyme and it typically includes the binding motif. The enzyme labile group links to the signalogenic substructure via a labile bond (LB) which is cleaved by the action of the marker enzyme separating the signalogenic substructure and the enzyme labile group. In some embodiments a linker is inserted between the signalogenic substructure and the enzyme labile group. Presence of the enzyme and thus the organism is detected by presence of a fluorogenic, precipitate that can be detected in single colonies.
priorityDate 2007-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ86AS5
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ55EU1

Total number of triples: 958.