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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6f0e32ac19ae429966474d25f5c76f86
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12M41-46
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6841
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-689
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 2017-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c293b005b70303c908cd25938ac6f239
publicationDate 2019-07-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-3510169-A1
titleOfInvention Method for detecting bacteria
abstract The present proposals relate to methods for detection of whole-cell bacteria, for example whole-cell pathogenic bacteria, in particular drug-resistant bacteria. These proposals also include apparatus and kits for use in such methods. Described is a method of detecting specific whole-cell bacteria, the method comprising: adding a probe composition to a sample comprising whole bacterial cells, the probe composition comprising a capture probe L-O1 and a signal probe X-=2, wherein L is at least one moiety that is one half of a binding pair, X is at least one signal moiety that provides an observable signal, and each O1 and O2 is independently a 15-150 nucleotide oligomer that is complementary to a portion of a nucleotide sequence of the specific bacteria; bringing the sample/probe composition mixture into contact with a substrate on which a moiety L' is immobilised wherein L' is complementary to and binds with the moiety L; washing the substrate to remove excess sample and probe composition; and detecting the observable signal.
priorityDate 2016-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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