http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S61182578-A

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-569
filingDate 1985-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_48b3ba6e070e1a2d99bca5f94b4bfc8e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2a8564f222d3250613269c4b23af825a
publicationDate 1986-08-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S61182578-A
titleOfInvention Method and reagent for quantitative determination of anti-streptolysin o antibody
abstract PURPOSE:To improve the accuracy of quantitative determination by mixing serum and the latex of an insoluble carrier which is sensitized with streptolysin O and has <0.2mum grain size in such a manner that the final concn. attains <0.05wt%, inducing a latex agglutination reaction by the antigen-antibody reaction and measuring light absorbency at 530-600nm wavelength. CONSTITUTION:The serum and the latex of the insoluble carrier which is sensitized with the streptolysin and has about 0.05-0.2mum grain size are mixed with a phosphoric acid buffer soln., etc. as a medium in such a manner that the final concn. of the insoluble carrier attains <0.05wt% to prepare a mixed liquid. The mixed liquid induces the latex agglutination reaction by the antigen- antibody reaction and the light absorbency of the reaction liquid after the reaction is measured by using the adequate wavelength of 530-600nm. The optical path length of the cell in the absorbency measurement is preferably about 5-10mm.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7759074-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0192885-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2006349838-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S63184063-A
priorityDate 1985-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 28.