http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2019149963-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_173bc2c63b34988699010ba05e5b1376
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-16
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6895
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6895
filingDate 2019-02-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_72cbfa158f58fe4fbc8e82a100e7f4ea
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4372fa866c074125dc6dd14fb5387a0
publicationDate 2019-08-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2019149963-A1
titleOfInvention Methods for detecting fungi in turf grass with a lamp assay having novel primer sets
abstract The present invention provides a method for detecting fungal DNA in a turf grass sample with a loop- mediated isothermal amplification (LAMP) assay which contains primers for fungal DNA of at least one turf pathogenic fungi selected from Sclerotinia homoeocarpa, Rhizoctonia solani spp., Pythium aphanidermatum, Gaeumannomyces graminis spp., Microdochium nivale spp., Magnaporthe poae, Colletotrichum graminicola, Colletotrichum cereale and Pythium ultimum var. ultimum, comprising: subjecting the turf sample to a LAMP reaction wherein the LAMP reaction uses a primer set of four or more nucleic acid sequences with each primer in the set having from 15 to 50 nucleic acids The primers useful in the present method are selected from specifically selected internal transcribed spacer regions or genes of the target fungi to provide improved assay results.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111893204-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111088395-A
priorityDate 2018-02-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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