Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_268be9afa00cf55b5aa72b1612151ecb http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0a9fdcdad4be7904a08a856f7eec3941 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-1405 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01L3-502 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N1-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01L2300-042 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01L2200-0605 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-150351 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N1-38 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-96 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-491 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-150755 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B5-150343 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N1-38 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-49 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-96 |
filingDate |
2016-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4ea1377023a0703d078e9d62bde3e496 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_170632eac29355992b1d99a6ba997183 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7697f085ec8868081fd272faa80c8bcb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ab95049d4096ba8059e42fc5b34b6213 |
publicationDate |
2018-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
JP-2018105828-A |
titleOfInvention |
Blood analysis method and blood test kit |
abstract |
The present invention provides a blood analysis method and a blood test kit for accurately determining a dilution ratio and quantitatively analyzing components. A step of diluting a collected blood sample with a diluent, a step of determining a dilution factor using a standard value of a standard component that is constantly present in blood, and a concentration of a target component in the blood sample A blood analysis method comprising the steps of: analyzing a blood from a blood sample diluted with a diluent, a first storage device containing a diluent, a collection device for collecting blood; The blood analysis method uses a member selected from the group consisting of a separation instrument for separating and collecting the sample, a holding instrument for holding the separation instrument, and a second storage instrument for containing the collected plasma. The blood analysis method of correcting the dilution factor after calculating in advance the amount of the standard component derived from the diluent and / or the amount of the standard component derived from at least one of the members that can be included in the diluent. [Selection figure] None |
priorityDate |
2016-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |