http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20180016178-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-533
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-544
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-533
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filingDate 2016-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_55e88795aff5492cd9e4c88dcb914ba0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2a651637412ca8465d7ff649037b2cb4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b289160cb0d56d0b7c40f6cf95cc10a1
publicationDate 2018-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20180016178-A
titleOfInvention Annexin V-fluorophore conjugates for real-time apoptosis fluorescence imaging and use thereof
abstract The present invention relates to annexin V-fluorescent dye conjugates and their uses for real-time apoptosis fluorescence imaging. Using the properties of the annexin V-fluorescent dye conjugates of the present invention, it is possible to detect apoptotic cells with a high signal-to-noise ratio without washing, so that cells undergoing apoptosis Only fluorescence can be detected more specifically. In addition, when the annexin V-fluorescent dye conjugate of the present invention is used, real-time apoptosis fluorescence image analysis and three-dimensional apoptosis analysis that could not be achieved with the existing annexin V-fluorescent dye conjugate can be performed And it is possible to shorten the analysis time and the analysis efficiency remarkably in the large-dose drug screening.
priorityDate 2016-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID171735
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426384181
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411319808

Total number of triples: 308.