http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009537013-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02A50-30 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-563 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K16-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-56983 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-569 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-569 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-53 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-536 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-543 |
| filingDate | 2007-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2009-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2009537013-A |
| titleOfInvention | Antigen capture anti-dengue IgA ELISA (ACA-ELISA) for detection of flavivirus specific antibodies |
| abstract | An antigen capture IgA enzyme immunoassay (ACA-ELISA) for the detection of anti-flavivirus IgA was developed. The assay uses a flavivirus lytic antigen, preferably a dengue lytic antigen captured by a monoclonal antibody. Anti-flavivirus IgA captured from the test serum is preferably detected using a rabbit anti-IgA labeled with a reporter group such as horseradish peroxidase (HRP). This assay was found to be at least 8 times more sensitive than the anti-human IgA capture ELISA (AAC-ELISA). The ACA-ELISA based on either serum or saliva was found to be more sensitive and rapid compared to the “golden rule” anti-dengue IgM detection technique. This can be used as a diagnostic tool for dengue confirmation in the early stage of infection. [Selection figure] None |
| priorityDate | 2006-05-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 57.