http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102721684-B

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Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8c90e762403eadedec292730a4743434
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-78
filingDate 2012-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e7d68ef09a19b7b45e7a49fdc4ba9e8f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_704a6a46035fe1195ad107568fd074d8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fb492a10297753679db03e5b7b34cf3e
publicationDate 2015-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102721684-B
titleOfInvention Two-step enzyme measuring method and measuring reagent for creatinine in blood serum
abstract The invention discloses a two-step enzyme measuring method and measuring reagents for creatinine in blood serum. The hydrogen peroxide generated by endogenous creatine is eliminated by utilizing catalase in a reagent 1 of the creatinine measuring reagents, and the catalase in the reagent 1 is suppressed by utilizing the catalase in a reagent 2 of the creatinine measuring reagents, so that the creatinine content in a sample is measured. The invention has the advantages that the phenomenon that the cost is increased because of oxidizing hydrogen peroxide by the catalase, so that the detection result is low in accuracy and precision is avoided.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3258273-A1
priorityDate 2012-05-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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