Lossless Three-Dimensional Parallelization in Digitally Scanned Light-Sheet Fluorescence Microscopy

We introduce a concept that enables parallelized three-dimensional imaging throughout large volumes with isotropic 300–350 nm resolution. By staggering high aspect ratio illumination beams laterally and axially within the depth of focus of a digitally scanned light-sheet fluorescence microscope (LSF...

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Detalles Bibliográficos
Autores principales: Dean, Kevin M., Fiolka, Reto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570909/
https://www.ncbi.nlm.nih.gov/pubmed/28839150
http://dx.doi.org/10.1038/s41598-017-08113-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570909/
https://www.ncbi.nlm.nih.gov/pubmed/28839150
http://dx.doi.org/10.1038/s41598-017-08113-8

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