ABERRATION CORRECTED BEAM SCANNING STIMULATED EMISSION DEPLETION MICROSCOPY

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dc.contributor.authorYoo, Hongkiko
dc.contributor.authorSong, Incheonko
dc.contributor.authorGweon, Dae-Gabko
dc.date.accessioned2010-02-10T06:22:18Z-
dc.date.available2010-02-10T06:22:18Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2008-
dc.identifier.citationINTERNATIONAL JOURNAL OF OPTOMECHATRONICS, v.2, no.4, pp.401 - 412-
dc.identifier.issn1559-9612-
dc.identifier.urihttp://hdl.handle.net/10203/16595-
dc.description.abstractWe present an aberration corrected beam scanning stimulated emission depletion (STED) microscopy. The beam scanning is essential to get images fast for practical usages in the biological applications. In this work the beam scanning method is applied to the STED microscopy. To maintain the imaging performance optimally, the aberration induced by the optic components, especially beam scanning parts, is corrected using adaptive optics. Thus, high resolution over the diffraction limit and high scanning speed are achieved without resolution and signal loss caused by the aberration.-
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherTAYLOR FRANCIS INC-
dc.titleABERRATION CORRECTED BEAM SCANNING STIMULATED EMISSION DEPLETION MICROSCOPY-
dc.typeArticle-
dc.identifier.wosid000270085400004-
dc.identifier.scopusid2-s2.0-56349163374-
dc.type.rimsART-
dc.citation.volume2-
dc.citation.issue4-
dc.citation.beginningpage401-
dc.citation.endingpage412-
dc.citation.publicationnameINTERNATIONAL JOURNAL OF OPTOMECHATRONICS-
dc.identifier.doi10.1080/15599610802564550-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorYoo, Hongki-
dc.contributor.localauthorGweon, Dae-Gab-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusFLUORESCENCE MICROSCOPY-
dc.subject.keywordPlusCONFOCAL MICROSCOPY-
dc.subject.keywordPlusRESOLUTION-
dc.subject.keywordPlusSYSTEM-
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