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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-53
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P21-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-566
filingDate 1997-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fe4c1d777f7dc4dab3e89d22cf3e074c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_265cc72d43145a474cbb41521c287484
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publicationDate 1999-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H11108925-A
titleOfInvention Prostate specific antigen measurement method
abstract (57) [Summary] (Modifications) [Problem] To measure the ratio of fPSA to tPSA directly without measuring fPSA and tPSA separately, A method for differentiating between prostate cancer and benign prostatic hyperplasia in a region where the amount of PSA is 3 to 10 ng / ml. A sample is contacted with a solid phase on which a first receptor having an affinity for both free and complexed prostate-specific antigens is immobilized on a carrier, and the prostate-specific antigen in the sample is contacted. A certain amount of antigen is selectively captured on the solid phase, the solid phase and the sample are separated, and a labeled second receptor having an affinity for free prostate-specific antigen is added to the separated solid phase. By contacting, the labeled substance is bound to the free prostate specific antigen contained in the entire amount of the prostate specific antigen captured on the solid phase, the solid phase and the liquid phase of the reaction mixture are separated, and the separated solid phase or liquid is separated. Determine the amount of labeled material in the phase.
priorityDate 1997-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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