http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2006098293-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9019c0ce5cb7b82c85e121f6cac86dce
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-53
filingDate 2004-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2dcbce5151e9ca32363eb5ce6388b0ea
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d91593a31d645f4a4f12ca3916d3b9bc
publicationDate 2006-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2006098293-A
titleOfInvention How to convert paralytic shellfish poison components
abstract PROBLEM TO BE SOLVED: To correctly determine the content of a PSP component even in the case of containing a N1-OH type PSP component with low detection sensitivity in detecting paralytic shellfish poison. The method for converting a paralytic shellfish venom component according to the present invention comprises dissolving an N1-OH type paralytic shellfish venom component in a neutral aqueous solution containing a heme-related component, and supplying the neutral aqueous solution with an electron donor. In order to reduce the N1 position of the paralytic shellfish poison component by quantitatively converting it into an N1-H type paralytic shellfish poison component by incubating the mixed solution, By converting an N1-OH type PSP component having low reactivity with an antibody into an N1-H type PSP component having high reactivity, it is possible to ensure quantitativeness by a simple analytical method such as ELISA. . [Selection] Figure 8
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priorityDate 2004-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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