http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2022242895-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_46570326040ec3afb9917a7e7799019f |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-533 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G06K9-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G06K19-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-533 |
| filingDate | 2021-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_434caad38615366593761d4e5f0e08c8 |
| publicationDate | 2022-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | WO-2022242895-A1 |
| titleOfInvention | Marker, method and device for analyzing a biological sample |
| abstract | A marker (100) for marking a predetermined structure (102) within a biological sample (902). The marker (100) comprises an affinity reagent (104) configured to attach to the predetermined structure (102), a linker structure (106) attached to the affinity reagent (104) and extending from the affinity reagent (104), and at least two different fluorescent dyes (110a, 110b, 110c, 110d, 110e) arranged at the linker structure (106). The linker structure (106) comprises at least one cleavage site (112a to 112d) arranged between the two fluorescent dyes (110a, 110b, 110c, 110d, 110e) or between a fluorescent dye and the linker structure (106). The linker structure (106) or the fluorescent dye can be cut at the cleavage site (112a to 112d) by a cleaving agent (200, 400) in order to remove at least one of the fluorescent dyes (110a, 110b, 110c, 110d, 110e) from the marker (100). |
| priorityDate | 2021-05-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 83.