http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H05113441-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6bfdf49224a405be1f7b653c56ebad94 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N30-88 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-72 |
| filingDate | 1991-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82ea7dec83f7145323347f169b677ecf |
| publicationDate | 1993-05-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H05113441-A |
| titleOfInvention | Analysis method of glycated hemoglobin |
| abstract | (57) [Summary] [Purpose] To provide a method for separating glycated hemoglobin and non-glycated hemoglobin in blood to efficiently analyze glycated hemoglobin, which is an optimal index for the diagnosis of diabetes and the follow-up of diabetic patients. To do. [Structure] First, the first liquid, the second liquid, and the third liquid are sequentially used to bring the sample into contact with the filler having a cation exchange group, and then to the filler having a boric acid exchange group, whereby non-saccharification is first performed. Hemoglobin and glycated hemoglobin are adsorbed on the cation exchange group, then glycated hemoglobin is adsorbed on the boric acid exchange group, and then glycated hemoglobin is eluted and separated. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2012111-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2015053-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2012111-A4 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8268625-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-114712894-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2015053-A4 |
| priorityDate | 1991-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 26.