http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1053248-B1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y10S435-975
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07K14-005
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K14-035
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filingDate 1998-02-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f3050a3ec5d3ff14c9d753e8f3e48ec9
publicationDate 2007-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1053248-B1
titleOfInvention Peptide structures and their use in diagnosis of herpes simplex virus type 2
abstract A multiply-displayed peptide structure is provided for the serodiagnosis of HSV-2 antibodies, preferably by ELISA. The structure has the formula (1)): [(X1)p-16aa sequence-(X2)q-Sp]n-core, wherein "16aa sequence" represents a sequence (SEQ ID NO: 68) - - Glu Glu Phe Glu Gly Ala Gly Asp Gly Glu Pro Pro - 1 5 10 - +TR - Glu Asp Asp Asp - 15 - X1 and X2 which may be the same or different represent from 1 to 6 non-interfering amino acid residues, which may be the same or different; Sp represents a spacer group extending outwardly from the core; n is at least 4; p is 0 or 1; q is 0 or 1; and the linkage between the core and the spacer group may be chemical or physical. Preferably p is 1, q is 1, X1 is Pro, n is 4, and the core is a branched lysine core, whereby the whole structure is a peptide. The monomeric peptides (X1)p-16aa sequence-(X2)q-(Sp)r, where r is 0 or 1 and their functional derivatives are useful intermediates in preparing the above structures.
priorityDate 1997-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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