http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2004089103-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ef3e73bf82e05dd388bd59b6da624736 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-415 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K39-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P37-08 |
filingDate | 2002-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c224b8ff26bfcb0315db7e2fc0ac2484 |
publicationDate | 2004-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2004089103-A |
titleOfInvention | Nucleic acid molecule encoding cedar pollen allergen protein |
abstract | An object of the present invention is to clone a gene encoding a cedar pollen allergen useful for hyposensitization therapy or diagnosis of cedar pollinosis patients. A cDNA was synthesized by reverse transcription using a random hexamer or oligo (dT) 17 primer using cedar pollen RNA as a template. Double-stranded DNA was synthesized from random cDNA using Klenow enzyme using primers synthesized based on conserved regions of several plants having high homology to the mountain cedar pollen allergen Jun a3. A partial DNA fragment of cedar pollen Cry j 3 was obtained by PCR using primers synthesized based on the above conserved region using this DNA as a template. The 5 'side was obtained by PCR using degenerate primers. And the 3 'side was obtained by the 3'-RACE method. From these, the gene sequence of all Cry j 3a was determined. [Selection diagram] None |
priorityDate | 2002-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 69.