http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2019075769-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_59a5d6ed219ca4a88ea1fc62fe730b6d
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-68
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filingDate 2017-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_edd21911da924b18e71917460d4187ed
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9788449bcbfccbd8572edf5411e72475
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publicationDate 2019-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2019075769-A1
titleOfInvention Method for detecting hypersensitive C-reactive protein
abstract A method for detecting a hypersensitive C-reactive protein comprises the following steps: 1) preparing a standard test sample by a sample diluent to obtain a luminescence signal value, and then using the standard concentration as an abscissa and the signal value as an ordinate Draw a standard curve; 2) prepare streptavidin magnetic beads, label buffer, biotinylated hs-CRP antibody and acridinium ester labeled hs-CRP antibody; 3) take appropriate amount of serum sample to be tested Adding to the reaction cup of the fully automatic luminescence immunoassay analyzer, and adding an appropriate amount of the biotin-labeled antibody, the acridinium ester-labeled antibody, and the streptavidin magnetic bead bath prepared in the step 2) to obtain the signal value of the serum sample to be tested, At the same time, an appropriate amount of the standard test sample is added to the reaction cup as a control for testing; 4) the signal value of the sample to be tested is then compared with the standard curve of step 1) to obtain a high-sensitivity C-reactive protein in the serum sample to be tested. concentration.
priorityDate 2017-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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