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dc.contributor.authorSparks, H
dc.contributor.authorDent, L
dc.contributor.authorBakal, C
dc.contributor.authorBehrens, A
dc.contributor.authorSalbreux, G
dc.contributor.authorDunsby, C
dc.date.accessioned2021-01-27T16:27:21Z
dc.date.issued2020-12-01
dc.identifier.citationBiomedical optics express, 2020, 11 (12), pp. 7204 - 7220
dc.identifier.issn2156-7085
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4324
dc.identifier.eissn2156-7085
dc.identifier.doi10.1364/boe.409781
dc.description.abstractWe present a new folded dual-view oblique plane microscopy (OPM) technique termed dOPM that enables two orthogonal views of the sample to be obtained by translating a pair of tilted mirrors in refocussing space. Using a water immersion 40× 1.15 NA primary objective, deconvolved image volumes of 200 nm beads were measured to have full width at half maxima (FWHM) of 0.35 ± 0.04 µm and 0.39 ± 0.02 µm laterally and 0.81 ± 0.07 µm axially. The measured z-sectioning value was 1.33 ± 0.45 µm using light-sheet FWHM in the frames of the two views of 4.99 ± 0.58 µm and 4.89 ± 0.63 µm. To qualitatively demonstrate that the system can reduce shadow artefacts while providing a more isotropic resolution, a multi-cellular spheroid approximately 100 µm in diameter was imaged.
dc.formatElectronic-eCollection
dc.format.extent7204 - 7220
dc.languageeng
dc.language.isoeng
dc.publisherOPTICAL SOC AMER
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.titleDual-view oblique plane microscopy (dOPM).
dc.typeJournal Article
dcterms.dateAccepted2020-10-28
rioxxterms.versionofrecord10.1364/boe.409781
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2020-12
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfBiomedical optics express
pubs.issue12
pubs.notesNot known
pubs.organisational-group/ICR
pubs.publication-statusPublished
pubs.volume11
pubs.embargo.termsNot known
dc.contributor.icrauthorBakal, Christopher
dc.contributor.icrauthorBehrens, Axel


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