DC Field | Value | Language |
---|---|---|
dc.contributor.author | C K Lim | - |
dc.contributor.author | J S Lee | - |
dc.contributor.author | Tai-Hwan Ha | - |
dc.contributor.author | I C Kwon | - |
dc.contributor.author | C H Ahn | - |
dc.contributor.author | S Y Park | - |
dc.date.accessioned | 2017-04-19T09:07:04Z | - |
dc.date.available | 2017-04-19T09:07:04Z | - |
dc.date.issued | 2007 | - |
dc.identifier.issn | 1010-6030 | - |
dc.identifier.uri | 10.1016/j.jphotochem.2006.12.002 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/7898 | - |
dc.description.abstract | In this work, we report a novel stimuli-sensitive probe working on the principle of the cleavage-induced fluorescent change via hydrophilicity control. In our Si-Py-Ac-PEG probe, cleavage of hydrophilic PEG moiety in acidic environment induces hydrophobic interaction of pyrenes to increase their excimer emission. Our fluorescent probe (Si-Py-Ac-PEG) was successfully applied to the spotting microarray and nanoparticle suspension to demonstrate the potential of biological applications, i.e. protein chip and bioimaging. | - |
dc.publisher | Elsevier | - |
dc.title | Cleavage-induced fluorescence change via hydrophilicity control: A new strategy for biological application | - |
dc.title.alternative | Cleavage-induced fluorescence change via hydrophilicity control: A new strategy for biological application | - |
dc.type | Article | - |
dc.citation.title | Journal of Photochemistry and Photobiology A-Chemistry | - |
dc.citation.number | 2 | - |
dc.citation.endPage | 154 | - |
dc.citation.startPage | 149 | - |
dc.citation.volume | 188 | - |
dc.contributor.affiliatedAuthor | Tai-Hwan Ha | - |
dc.contributor.alternativeName | 임창근 | - |
dc.contributor.alternativeName | 이진성 | - |
dc.contributor.alternativeName | 하태환 | - |
dc.contributor.alternativeName | 권익찬 | - |
dc.contributor.alternativeName | 안철희 | - |
dc.contributor.alternativeName | 박수영 | - |
dc.identifier.bibliographicCitation | Journal of Photochemistry and Photobiology A-Chemistry, vol. 188, no. 2, pp. 149-154 | - |
dc.identifier.doi | 10.1016/j.jphotochem.2006.12.002 | - |
dc.subject.keyword | biomedical imaging | - |
dc.subject.keyword | cleavage | - |
dc.subject.keyword | excimer emission | - |
dc.subject.keyword | hydrophilicity control | - |
dc.subject.keyword | microarray | - |
dc.subject.local | biomedical imaging | - |
dc.subject.local | Biomedical imaging | - |
dc.subject.local | cleavage | - |
dc.subject.local | excimer emission | - |
dc.subject.local | hydrophilicity control | - |
dc.subject.local | microarray | - |
dc.subject.local | microarry | - |
dc.subject.local | Microarray | - |
dc.subject.local | microarrays | - |
dc.description.journalClass | Y | - |
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