http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H02119798-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5f6a891d6ea05c54f839b01a20d1c3bc |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-37 |
| filingDate | 1988-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0d47f044ef00a8bdc8220142a0a0d4e5 |
| publicationDate | 1990-05-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H02119798-A |
| titleOfInvention | Method for measuring activity of urokinase inhibitor |
| abstract | PURPOSE: To rapidly and readily measure the activity of the subject compound useful for diagnosing abnormal fibrinolysis, etc., with high sensitivity and excellent specificity by removing urokinases using an affinity column, then adding urokinase and synthetic substrate, etc., thereto and measuring the amount of the neutralized urokinase. n CONSTITUTION: A specimen (e.g., human blood plasma) is passed through an affinity column filled with agarose particles immobilizing antiurokinase house rabbit immnnoglobulin G, etc., to remove urokirkase and urokinase-urokinase inhibitor complex in the specimen. A known amount of urokinase is then added and reacted with a urokinase inhibitor in the specimen and the residual urokinase is subsequently measured with a synthetic substrate or plasminogen- containing fibrin plate. Thereby, the activity of the urokinase inhibitor in the specimen is measured from the amount of the neutralized urokinase. n COPYRIGHT: (C)1990,JPO&Japio |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5496879-A |
| priorityDate | 1988-10-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 41.