| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ec5b8c0fc1f827c1360a8f5ea5652225 |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2500-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2333-4709
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2500-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2800-2821 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-6845
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01D15-325
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-6896
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N30-89 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-557 |
| filingDate |
2014-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_04e4b0fa2329e57a2e73b828b790bd56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ccc6ab3086a8386a35becbe10a479553
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_640938bbb7df2b00c23b0535eb0c668a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b69fe74b6b39cf790aefc5278c9d804 |
| publicationDate |
2015-01-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
WO-2015003674-A2 |
| titleOfInvention |
Method for the quantitative characterisation of amyloid and/or aggregating peptides and/or proteins in a sample |
| abstract |
The invention relates to a method for the quantitative characterisation of amyloid and/or aggregated peptides and/or proteins in a sample, comprising the following steps: preparing a sample containing an amyloid and/or aggregated peptide and/or protein having at least one aggregate size and shape; adding an active ingredient to be analysed to the sample solution; separating the amyloid and/or aggregated peptides and/or proteins from one another according to their aggregate size and shape; optionally completely denaturing the amyloid and/or aggregated peptides and/or proteins of a particular fraction into monomer units; comparing against control values without the active ingredient in order to determine the change in concentration of the peptide and/or protein units in at least one fraction. |
| priorityDate |
2013-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |