http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-209778828-U

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6192d9c16465d28950ed9ffe6842f23d
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12M1-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12M1-00
filingDate 2019-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_138fda89f3158f2f1542a7fc9eb0f0a0
publicationDate 2019-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-209778828-U
titleOfInvention centrifugal micro-fluidic chip structure and nucleic acid analysis device
abstract The application relates to a centrifugal micro-fluidic chip structure and a nucleic acid analysis device, wherein the centrifugal micro-fluidic chip structure comprises a chip substrate, a sample adding cavity, a gas outlet, a sample enrichment and lysis cavity, a first waste liquid cavity, a first capillary valve, a dilution cavity, a second capillary valve, a PCR amplification cavity and a second waste liquid cavity; the sample adding cavity is provided with a sample adding hole and is communicated with the sample enrichment and cracking cavity through a sample adding cavity circulation pipeline; the sample enrichment cracking cavity is communicated with the first waste liquid cavity through a cracking cavity circulation pipeline, is also communicated with a cracking cavity mixing pipeline through a first capillary valve, and is communicated with the dilution cavity through a cracking cavity mixing pipeline; the dilution cavity is communicated with the PCR amplification cavity and the second waste liquid cavity through a second capillary valve, and the first waste liquid cavity and the second waste liquid cavity are communicated with the gas outlet through gas circulation pipelines respectively. The PCR amplification technology can be applied to the centrifugal microfluidic technology to realize molecular diagnosis based on PCR amplification, and a large molecular diagnosis laboratory is not required to be built, and a large amount of manual operation is not required to be adopted.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113583839-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111604096-A
priorityDate 2019-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 18.