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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a25020e2d0af2f96f0432c19fbd21ea7
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-543
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-577
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-72
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-72
filingDate 2009-05-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e23970ef3291bd1f052b69ad59293d68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9bcb97419224264bbd3d3d45b28840c6
publicationDate 2015-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-101900725-B
titleOfInvention Method for detecting trace protein or polypeptide by utilizing positive-feedback enzyme reaction amplification system
abstract The invention belongs to the field of protein or polypeptide detection and discloses a method for detecting trace protein or polypeptide by utilizing a positive-feedback enzyme reaction amplification system. The method adopts an enzyme-linked immunosorbent assay method combining a positive-feedback enzymatic reaction amplification system and an enzyme reaction kinetic analysis method to detect the protein or polypeptide to be detected. The method has the advantages that the detection sensitivity can reach 1-50 fmol/L and is improved by 4-5 orders of magnitude compared with the conventional ELISA sensitivity.
priorityDate 2009-05-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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