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3D structured illumination microscope using a spinning disk [Invited].
Zhang, Youchang; Asghari, Parisa; Scriven, David R L; Moore, Edwin D W; Chou, Keng C.
Afiliación
  • Zhang Y; Department of Chemistry, Life Sciences Institute, University of British Columbia, Vancouver, BC V6T 1Z1, Canada.
  • Asghari P; Department of Cellular and Physiological Sciences, Life Sciences Institute, University of British Columbia, Vancouver, BC V6T 1Z3, Canada.
  • Scriven DRL; Department of Cellular and Physiological Sciences, Life Sciences Institute, University of British Columbia, Vancouver, BC V6T 1Z3, Canada.
  • Moore EDW; Department of Cellular and Physiological Sciences, Life Sciences Institute, University of British Columbia, Vancouver, BC V6T 1Z3, Canada.
  • Chou KC; edwin.moore@ubc.ca.
Biomed Opt Express ; 14(11): 5710-5719, 2023 Nov 01.
Article en En | MEDLINE | ID: mdl-38021136
ABSTRACT
Three-dimensional (3D) structured illumination microscopy (SIM) improves spatial resolution by a factor of two in both lateral and axial directions. However, the adoption of 3D SIM is limited by low imaging speed, susceptibility to out-of-focus light, and likelihood of reconstruction errors. Here we present a novel approach for 3D SIM using a spinning disk. The disk generates a 3D lattice illumination pattern on the sample and optically reconstructs super-resolved images in real time. This technique achieves a 2-times resolution improvement with a speed up to 100 frames per second while physically rejecting 90% of the background signal.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Biomed Opt Express Año: 2023 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Biomed Opt Express Año: 2023 Tipo del documento: Article País de afiliación: Canadá
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