<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sparks H</submitter><funding>Cancer Research UK</funding><funding>Francis Crick Institute</funding><funding>The Francis Crick Institute</funding><funding>Engineering and Physical Sciences</funding><funding>Wellcome Trust</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>7204-7220</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7747899</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(12)</volume><pubmed_abstract>We 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.</pubmed_abstract><journal>Biomedical optics express</journal><pubmed_title>Dual-view oblique plane microscopy (dOPM).</pubmed_title><pmcid>PMC7747899</pmcid><funding_grant_id>FC001317</funding_grant_id><funding_grant_id>20146</funding_grant_id><funding_grant_id>10317</funding_grant_id><funding_grant_id>FC001039</funding_grant_id><funding_grant_id>21144</funding_grant_id><funding_grant_id>C37275/A20146</funding_grant_id><funding_grant_id>EP/T003103/1</funding_grant_id><funding_grant_id>10039</funding_grant_id><pubmed_authors>Behrens A</pubmed_authors><pubmed_authors>Dunsby C</pubmed_authors><pubmed_authors>Sparks H</pubmed_authors><pubmed_authors>Bakal C</pubmed_authors><pubmed_authors>Dent L</pubmed_authors><pubmed_authors>Salbreux G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dual-view oblique plane microscopy (dOPM).</name><description>We 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.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Dec</publication><modification>2026-07-09T11:05:41.205Z</modification><creation>2026-07-09T10:37:42.272Z</creation></dates><accession>S-EPMC7747899</accession><cross_references><pubmed>33408991</pubmed><doi>10.1364/BOE.409781</doi></cross_references></HashMap>