http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105648055-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-686
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-689
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-10
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-686
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-11
filingDate 2016-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2019-05-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105648055-B
titleOfInvention A kind of fowl source salmonella multiple PCR detection kit and its nondiagnostic detection method
abstract The invention discloses a kind of fowl source salmonella multiple PCR detection kit and its nondiagnostic detection methods.The kit includes 10 × PCR buffer, 2.5 U/ μ l Taq Archaeal dna polymerase, 10Mm dNTPs, multiple PCR detection primer group, positive control and negative control, the positive control include Bacterium enteritidis ATCC13076, salmonella typhimurium ATCC14028, avian infectious bronchitis nephritis virus ATCC9184 genomic DNA;The negative control is sterilizing distilled water.The invention also discloses a kind of multiple PCR methods using kit detection fowl source salmonella.The method of the present invention has the advantages that quick, simple, high specificity, high sensitivity, it is reacted by a PCR, three kinds of salmonellas can be used for quickly detecting and parting, it is detected compared to traditional serological typing and regular-PCR, there is greater advantage in terms of testing cost between when detecting, be suitable for batch detection.
priorityDate 2016-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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