Light microscopy of proteins in their ultrastructural context
Imaging specific proteins in the ultrastructural context largely relies on correlative light/electron microscopy, but fluorophore incompatibility and registration issues limit its use. Here the authors develop an expansion microscopy method with pan-labeling of the proteome to obtain EM-equivalent l...
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Formato: | article |
Lenguaje: | EN |
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Nature Portfolio
2020
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Acceso en línea: | https://doaj.org/article/4d8ba5c29a00481891dbe1df9367f3e0 |
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