Multiphoton structured thin-plane imaging with a single optical path

Cited 2 time in webofscience Cited 0 time in scopus
  • Hit : 545
  • Download : 0
DC FieldValueLanguage
dc.contributor.authorYu, Jiun-Yannko
dc.contributor.authorKim, Jonghyunko
dc.contributor.authorHolland, Daniel B.ko
dc.contributor.authorMou, Yunko
dc.contributor.authorChiu, Huiko
dc.contributor.authorBlake, Geoffrey A.ko
dc.contributor.authorLee, Wonheeko
dc.contributor.authorGuo, Chin-Linko
dc.date.accessioned2018-11-22T07:06:34Z-
dc.date.available2018-11-22T07:06:34Z-
dc.date.created2018-11-19-
dc.date.created2018-11-19-
dc.date.created2018-11-19-
dc.date.issued2018-11-
dc.identifier.citationOPTICS LETTERS, v.43, no.21, pp.5271 - 5274-
dc.identifier.issn0146-9592-
dc.identifier.urihttp://hdl.handle.net/10203/246880-
dc.description.abstractOptical sectioning has become an indispensable technique for high-speed volumetric imaging in the past decade. Here we present a novel optical-sectioning method that produces a thin plane of illumination by exploiting the spatial and temporal properties of multiphoton excitation. Critically, the illumination and detection share the same optical path, as in a conventional epi-fluorescence microscope configuration. Therefore, the imaged sample can be prepared as for standard fluorescence microscopy. Our method also leads to a laterally structured illumination pattern, and this feature can be utilized in structured illumination microscopy to further enhance the imaging performance. We show an example of such an approach, which achieves axial resolution finer than confocal microscopy. We also demonstrate the potential of the new method for biological applications by performing three-dimensional imaging of living Caenorhabditis elegans. (C) 2018 Optical Society of America-
dc.languageEnglish-
dc.publisherOPTICAL SOC AMER-
dc.subjectFLUORESCENCE MICROSCOPY-
dc.subjectILLUMINATION MICROSCOPY-
dc.subjectRESOLUTION-
dc.subjectORGANISMS-
dc.subjectDEEP-
dc.titleMultiphoton structured thin-plane imaging with a single optical path-
dc.typeArticle-
dc.identifier.wosid000448939000026-
dc.identifier.scopusid2-s2.0-85056086469-
dc.type.rimsART-
dc.citation.volume43-
dc.citation.issue21-
dc.citation.beginningpage5271-
dc.citation.endingpage5274-
dc.citation.publicationnameOPTICS LETTERS-
dc.identifier.doi10.1364/OL.43.005271-
dc.contributor.localauthorLee, Wonhee-
dc.contributor.nonIdAuthorYu, Jiun-Yann-
dc.contributor.nonIdAuthorHolland, Daniel B.-
dc.contributor.nonIdAuthorMou, Yun-
dc.contributor.nonIdAuthorChiu, Hui-
dc.contributor.nonIdAuthorBlake, Geoffrey A.-
dc.contributor.nonIdAuthorGuo, Chin-Lin-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusFLUORESCENCE MICROSCOPY-
dc.subject.keywordPlusILLUMINATION MICROSCOPY-
dc.subject.keywordPlusRESOLUTION-
dc.subject.keywordPlusORGANISMS-
dc.subject.keywordPlusDEEP-
dc.subject.keywordPlusFLUORESCENCE MICROSCOPY-
dc.subject.keywordPlusILLUMINATION MICROSCOPY-
dc.subject.keywordPlusRESOLUTION-
dc.subject.keywordPlusORGANISMS-
dc.subject.keywordPlusDEEP-
Appears in Collection
NT-Journal Papers(저널논문)
Files in This Item
There are no files associated with this item.
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 2 items in WoS Click to see citing articles in records_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0