http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101687001-B1

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filingDate 2015-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2016-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8712d0200796a3c50bc4d38167ea32a2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_442c1801e614ce89d2bbf8e78418e283
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publicationDate 2016-12-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-101687001-B1
titleOfInvention Method for improving fluorescence intensity of flow cytometric analysis by localization of a green fluorescent protein into chloroplasts
abstract Disclosed is a method for increasing fluorescence intensity in flow cytometry through chloroplast localization. According to the present invention, the use of the method for increasing fluorescence intensity in the flow cytometry through chloroplast localization brings an increase in fluorescence intensity at least 8 times than cytoplasmic localization, as well as an increase in transformation ratio at least more than 4.5 times that that of cytoplasmic localization. In addition, by using the method for increasing fluorescence intensity in the flow cytometry through chloroplast localization, according to the present invention, expression of outstanding fluorescence intensity is possible even with a small amount less than one tenth of an amount of existing DNA (100-130 g) used therefor.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-102088178-B1
priorityDate 2015-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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