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filingDate 2021-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e2b0da648229e5638110c1cf65514bce
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e846a277bf88bf46e59936b0c2d3278b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7f41b909d8d89919c7b142182b7cdc49
publicationDate 2022-10-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-4074839-A1
titleOfInvention Optimized oligonucleotide tx probe for a multiplexing analysis of nucleic acids and a multiplexing method
abstract The present invention provides a, preferably fully automated and/or multiplex, method for the simultaneous detection of a plurality of molecular genetic analytes in a collective and continuous reaction set up and at least one analyte specific oligonucleotide TX probes with a cleavable hydrolysis product for use in said method. Through the method the plurality of cleavable hydrolysis products is specifically released by a nuclease from the respective TX probes. Following a separation step, preferably in a capillary electrophoresis, for each hydrolysis product a clear and distinguishable from others signal is achieved. Each separated hydrolysis product respectively results in a signal enabling the qualitative and/or quantitative detection of each analyte comprising a molecular variant, e.g. single nucleotide polymorphism (SNP), deletion-insertion polymorphism (DIP) or other, respectively, that was targeted specifically by the plurality of TX probes. Preferably, the method is suitable to detect qualitatively and/or quantitatively small molecular variants as such SNP.
priorityDate 2021-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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