http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1387172-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a722744e77c81c5f5cf415087e2ee92b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_974449494c10d67e34f1acfa22bdb358
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-569
filingDate 1998-09-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8b87c5b44ce31445b4098ca4eab616d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8ea3690f0810266a2fe376a56c9c3026
publicationDate 2004-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1387172-A2
titleOfInvention Bovine viral diarrhea virus serum antigen capture immunoassay
abstract The invention disclosed herein presents an antigen-capture immunoassay that utilizesnserum, plasma, milk, urine, saliva, or other bodily fluid samples to identify cattle infectednwith the Bovine Viral Diarrhea Virus (BVDV). The results of this assay allow anneffective, reliable, quick, and cost efficient way to identify, and thereby remove, infectedncattle and/or other ruminants from otherwise uninfected herds. The BVD virus causes annacute enteric disease with a variety of clinical manifestations, and is closely related tonsheep border disease virus (BDV) and hog cholera virus (HCV). The traditional method ofndetecting infected animals, including persistently infected (PI) carriers, has been throughn.the .use of virus isolation procedures. While .this older test methodology can detectninfected animals, the virus isolation test can only be performed by highly trainedntechnicians in a highly specialized laboratory facility. The kit disclosed herein usesnELISA methodology, employs the BVDV antigen specific monoclonal antibody 15.c.5,nand requires at least 100 µl of sample per assay.
priorityDate 1997-09-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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