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Imaging Subcellular Dynamics with Fast and Light-Efficient Volumetrically Parallelized Microscopy

In fluorescence microscopy, the serial acquisition of 2D images to form a 3D volume limits the maximum imaging speed. This is particularly evident when imaging adherent cells in a light-sheet fluorescence microscopy format, as their elongated morphologies require ~200 image planes per image volume....

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Dades bibliogràfiques
Publicat a:Optica
Autors principals: Dean, Kevin M., Roudot, Philippe, Welf, Erik S., Pohlkamp, Theresa, Garrelts, Gerard, Herz, Joachim, Fiolka, Reto
Format: Artigo
Idioma:Inglês
Publicat: 2017
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5609504/
https://ncbi.nlm.nih.gov/pubmed/28944279
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1364/OPTICA.4.000263
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