http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2220785-A1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_22bc1750d9ebc8e9491183799fb333e3
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6809
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 1997-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f68d1e65fcc90a3f69ae34dae9c10415
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c5789b1c589383f9a8780fc97815b5b6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a7b2c2d02a3e5c2d4fc3c0f61bbccb28
publicationDate 1999-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2220785-A1
titleOfInvention Selective technique for rapid identification of proteins and genes and uses thereof
abstract A method relying on synthetic oligonucleotides as ligand for the parallel positive and negative selection for identifying and isolating target molecules that are differentially expressed in a plurality of biological system. These ligands comprise a randomized sequence region flanked by defined and fixed 5' and 3' regions. This method comprises many repetitive steps of incubation of target molecules from two systems with a pool of ligands, followed by a separation and an amplification of the ligands that bind in one system, and do not bind in the other system. The steps are repeated as many times as required to find ligands that bind specifically to the target molecules from system A but do not bind to the target molecules from system B. This method may be used as a very sensitive diagnostic tool since the final pool of ligands can identify target molecules that are different between normal vs pathological systems.
priorityDate 1997-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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