http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2013035703-A1
Outgoing Links
Predicate | Object |
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classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2021-6439 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2333-70596 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N21-6428 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-56966 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-582 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-57492 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-17 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-64 |
filingDate | 2012-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2015-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-WO2013035703-A1 |
titleOfInvention | Biological substance detection method |
abstract | The present invention relates to a method for detecting biological material specifically from a pathological section, in the case of performing simultaneous staining of immunostaining using a fluorescent label and morphological observation staining using a staining agent for morphological observation. Provided is a method capable of appropriately determining fluorescence observation and immunostaining results even when the fluorescent label or staining agent is deteriorated by irradiation with excitation light. In the biological material detection method according to the present invention, when observing the fluorescent label used for immunostaining, the luminance retention rate of the immunostained portion is in the range of 80% to 120% of the luminance retention rate of the morphology observation stained portion. It is characterized by that. |
priorityDate | 2011-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 80.