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High-resolution in-depth imaging of optically cleared thick samples using an adaptive SPIM
Today, Light Sheet Fluorescence Microscopy (LSFM) makes it possible to image fluorescent samples through depths of several hundreds of microns. However, LSFM also suffers from scattering, absorption and optical aberrations. Spatial variations in the refractive index inside the samples cause major ch...
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| Udgivet i: | Sci Rep |
|---|---|
| Main Authors: | , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Nature Publishing Group
2015
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4649629/ https://ncbi.nlm.nih.gov/pubmed/26576666 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep16898 |
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