http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-201211539-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7557c3288f71b0487c2efdd3945ecd7c
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-569
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N35-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N35-10
filingDate 2011-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_53bf709147b1a1bfa803e727fc3573be
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_afe754de62c5caf34e703ba2f482a8b3
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9f6f02296950e07fe7160e4bcaf0683c
publicationDate 2012-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-201211539-A
titleOfInvention LOC device for pathogen detection and genetic analysis with chemical lysis, incubation and tandem nucleic acid amplification
abstract A lab-on-a-chip (LOC) device for pathogen detection and genetic analysis of a biological sample, the LOC device having an inlet for receiving the sample, a supporting substrate, a plurality of reagent reservoirs, a lysis section for lysing pathogens and leukocytes in the sample to release the genetic material therein, the lysis section being in fluid communication with one of the reagent reservoirs containing a lysis reagent for lysing the pathogens and leukocytes in the lysis section, an incubation section downstream of the lysis section, the incubation section being in fluid communication with one of the reagent reservoirs containing enzymes for enzymatic reaction with the genetic material, a first nucleic acid amplification section downstream of the incubation section for amplifying first nucleic acid sequences in the genetic material, and, a second nucleic acid amplification section downstream of the first nucleic acid amplification section for amplifying second nucleic acid sequences in the amplicon from the first nucleic acid amplification section, wherein, the lysis section, the incubation section, the first nucleic acid amplification section and the second nucleic acid amplification section are all supported on the supporting substrate.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-I721680-B
priorityDate 2010-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID29386
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP75542
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID2656962
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID881822
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ3KSM3
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ8P778
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID3663
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP0AGE3
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID29672533
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID447566140
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ00566
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID56568104
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID58016173
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP51608
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9PKZ4
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ814G6
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID11072
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ4VR99
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID1024145
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ95LG8
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP47337
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID1487543
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ88QK5
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP66846
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID5739977
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ8ZJ06
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP42543
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP66855

Total number of triples: 338.