http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2673623-A1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8e9e28204ce5b58ff544f7ffcb52a6ec
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2333-96447
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-86
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-86
filingDate 2007-12-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d12f62bc1821a3b563bd661369a21cc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b91fbc9070049f67adc9981cbe3a08d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e97528183a562a0fd3756b8f12e76ccb
publicationDate 2008-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2673623-A1
titleOfInvention Method for measuring the concentration of activated factor vii (fviia) in a sample
abstract The present invention relates to a method for in vitro or ex-vivo measurement of FVII concentration in a sample, comprising the steps of: a) mixing said sample with human plasma lacking FVII and at least one other selected factor among FVIII, FIX and FXI; b) adding initiator components of the thrombin generation reaction comprising a source of calcium ions, a phospholipid agent and tissue factor; c) performing a thrombin generation test (TGT) on the reaction medium thus obtained to obtain a thrombinogram providing parameters; d) comparing at least one of the thrombinogram parameters with a homologous parameter of standard thrombograms, each standard thrombogram being obtained with a fixed standard concentration of FVIIa in said reaction medium, ranging from 1 μM to 5 nM, and e) deducing from step d) a measurement of the FVIIa concentration of the sample in said range.
priorityDate 2006-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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