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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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| Опубликовано в: : | Sci Rep |
|---|---|
| Главные авторы: | , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Nature Publishing Group UK
2017
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5570909/ https://ncbi.nlm.nih.gov/pubmed/28839150 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-08113-8 |
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