| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_60e66be87630d7cef0ce770e1d898eec |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2021-6439 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N21-6428
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N21-64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-569
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-582
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-04 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-64 |
| filingDate |
2020-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a74d24d29c66a6c20a911bd4f118b968
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_92c592cd03fb913ab96446fa7924ebe8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e7a2a884f95b6c36efd6ee5503b96a86
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e52b7d2c35052d0237926bcdd4118d81
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ea6819c387b08f6a966ff8f8856a43ad
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2dda6f4cd10d201af0cffa7645b6de1f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1642d4ca3827eb23d72cb4b69258329
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8f6d7dc65f36e37b51d42231f18833ca |
| publicationDate |
2022-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
US-2022307063-A1 |
| titleOfInvention |
Method for analyzing microbial flora |
| abstract |
A method for analyzing a microbiota, comprising (1) dissolving a probe capable of non-specifically interacting with a plurality of microorganisms in a plurality of solvents having different ionic strengths and pH levels, wherein the probe comprises: (a) a cationic polymer and (b) an environment-sensitive fluorophore; (2) adding a test sample containing the microbiota to a plurality of probe solutions prepared in the step (1), thereby microorganisms in the test sample and the probe are interacted non-specifically; (3) measuring fluorescence intensities of the plurality of probe solutions to which the test sample has been added in the step (2); and (4) comparing the pattern of fluorescence intensities obtained in the step (3) with the pattern of fluorescence intensities obtained from a reference sample. |
| priorityDate |
2019-06-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |