http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S613066-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-68
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-68
filingDate 1984-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e1c98b659ca083b35430f2c170e21180
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9120cd07079929f86b397bba91c4e950
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1291fbdf320f9a13fe536eefd3dfaeb1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8ef0613fdfff42da47e54f7fd074f901
publicationDate 1986-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S613066-A
titleOfInvention Assay of thiol group reacting group
abstract PURPOSE:To realize a highly reproducible assay with a simple operation, by making N-(2,4-dinitrophenyl) cysteine react with a substance containing a thiol group reacting group. CONSTITUTION:N-(2,4-dinitrophenyl) cysteine is made to react with a substance containing a thiol group reacting group and the absorbance derived from N-2,4- dinitrophenyl group in the resultant product is measured to assay the thiol group reacting group. The thiol group reacting group herein used is a maleimide group, 2,5-dioxyso-3-cyclohexenyl group, iodoacetyl group, bromoacetyl group or chloroacetyl group and the substance containing the thiol group reacting group is water-soluble protein introducing the thiol group reacting group. This method eliminates troublesome procedure for preventing errors due to disulfide conversion as in the case of using a thiol compound thereby making it sufficiently applicable for industrial production basis.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5576216-A
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priorityDate 1984-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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