http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20130054476-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_95363fc2cf0b49e7a4aef32d7cb692a1
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-04
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11
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filingDate 2011-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a1b990aaaa72be5284064851bd81f93e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d7cea328bf7151b0257c76ca7745dedd
publicationDate 2013-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20130054476-A
titleOfInvention Oligonucleotides and kits comprising the same are complementary to the Furizium Gramniarum assay gene used for quantitative reverse transcriptase chain reaction under various conditions
abstract The present invention relates to oligonucleotides and kits that are complementary to optimal assay genes for detecting Futurium Graminariaum, and more particularly to normalized Futurium Graminaria assay genes used for qRT-PCT under various conditions. The present invention relates to a complementary oligonucleotide (primer) and a kit for effectively detecting the bacterium comprising the same. Oligonucleotides complementary to the Fuzium Graminariaum assay gene used for quantitative reverse transcriptase chain reaction under various conditions of the present invention include consecutive nucleotides of nucleic acid complementary to any one or more of SEQ ID NO: 1 to SEQ ID NO: 16 It is characterized by having a length of 15 to 30 nucleotides selected from oligonucleotides. In addition, according to a preferred embodiment of the present invention, it is characterized in that it provides a kit for detecting Fujrium Grammiarum comprising any one or more of the above oligonucleotides. By using the oligonucleotide for detecting Futurium Graminirum of the present invention, Futurium Graminirum bacteria can be effectively detected under various conditions such as mycelial growth, sexual reproduction, and fungal toxin production (AG), and qRT- PCR can be used to identify suitable assay genes for normalized detection and to assay the bacteria faster and faster using complementary primers.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20170014230-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-115852014-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-115852014-A
priorityDate 2011-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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