http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H0552848-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-543
filingDate 1991-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_18e86bf74f1f007b963ee8b3e115d7e4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cef40d77ef9666271edcd44743751809
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_571829786789a0e5c0741bba89960d46
publicationDate 1993-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0552848-A
titleOfInvention Immunoassays and devices
abstract (57) [Summary] [Purpose] In immunoassays utilizing the antigen-antibody reaction, the fluorescence intensity is detected for each aggregation to accurately grasp the aggregation state and improve the measurement sensitivity. [Structure] Fluorescent fine particles are used as a reaction reagent, the reaction liquid after the reaction is introduced into a flow cell, and light is irradiated to the reaction liquid. The aggregation state is measured by detecting the fluorescence generated from the fine particles in the sample and having different intensity for each aggregation. [Effect] Simple operation and highly sensitive measurement can be performed. The conventional reagent production technology can be used as it is.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010223802-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-4796265-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-1317394-C
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009258034-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0196868-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010190880-A
priorityDate 1991-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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