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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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| Pubblicato in: | Optica |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2017
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| Soggetti: | |
| Accesso online: | 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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