http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109295242-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-158
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02A50-30
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-689
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-686
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-689
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-686
filingDate 2018-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-109295242-B
titleOfInvention Primer pair and kit for detecting trimethylamine production gene
abstract The invention discloses a primer pair and a kit for detecting a trimethylamine-producing gene. Based on the screened bacteria from the intestinal tract Clostridium saccharolyticum The trimethylamine producing gene of (a) is highly expressed in a human body and is named as a cutC gene. The gene sequence is shown in SEQ ID NO.1, a primer pair combination with specificity and ideal quantitative effect is found, and a detection kit is designed. The method effectively overcomes the defect of detecting the atherosclerosis risk genes in the intestinal bacteria in the prior art, and can improve the prediction rate of atherosclerosis diseases. The kit is suitable for all types of fluorescent quantitative gene amplification instruments on the market at present, has high sensitivity, high speed and accuracy in quantification, good stability, good application prospect and high industrial utilization value.
priorityDate 2018-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 23.