http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2008124098-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-6896
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-68
filingDate 2008-04-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d7e44778566f1bb69cd7f0fbbc75f621
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_53abc4300604a24cd8f39c9171ebc82c
publicationDate 2008-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2008124098-A1
titleOfInvention Prion assay
abstract The invention relates to an assay method for detecting the presence of PrPSc using at least one sequence-specific protease for a substantially complete digestion of the proteins in a sample, leaving the octarepeat region in both PrPSc and PrPC intact, leaving the protease-resistant core of PrPSc intact and remain connected to the octarepeat region, while digesting away at least part of the amino acid sequences in PrPC corresponding to the protease-resistant core in PrPSc. The method further comprises a step of inhibiting further digestion by the protease, a step of denaruration, and a step of detecting the presence of PrPSc using at least two binding partners, a first binding partner and a second binding partner, wherein the first binding partner specifically binds an epitope in the amino-proximal region, and the second binding partner specifically binds an epitope within a region of the protease-resistant core of PrPSc that has been cleaved away in PrPC. The invention also relates to a kit comprising reagents that can be used in the assay method.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2010084201-A1
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priorityDate 2007-04-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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