http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007077255-A1

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_292b0d28b8d6f542e51229df197a8de5
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-385
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-385
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K39-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H21-04
filingDate 2006-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_62d091214d5e78df43dcf217e1b0fb05
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_291d2b93444ec2c011743ade1132b31b
publicationDate 2007-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2007077255-A1
titleOfInvention Isolation and characterization of a cDNA clone encoding one IgE-binding fragment of Penicillium brevicompactum
abstract Pen b 26 was isolated as an allergen of Penicillium brevicompactum, which is known to be one of the major source of indoor fungal allergies. Pen b 26 was isolated and cloned into Escherichia coli as an N-terminus his-tagged fusion protein, which had a calculated molecular weight of 14.9 kDa while the native Pen b 26 was 11 kDa. The over-expressed fusion protein migrated at about 20 kDa on SDS-PAGE although its analysis by mass spectroscopy confirmed its calculated size. The IgE antibodies in the sera of >25% Penicillium -allergic individuals showed positive reaction to the purified fusion protein. Pen b 26 was also identified as a 60S ribosomal P1 phospho-protein. This invention includes a cDNA sequence from which the recombinant allergen was produced.
priorityDate 2005-10-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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