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Ultrafast superresolution fluorescence imaging with spinning disk confocal microscope optics

Most current superresolution (SR) microscope techniques surpass the diffraction limit at the expense of temporal resolution, compromising their applications to live-cell imaging. Here we describe a new SR fluorescence microscope based on confocal microscope optics, which we name the spinning disk su...

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Detalhes bibliográficos
Publicado no:Mol Biol Cell
Main Authors: Hayashi, Shinichi, Okada, Yasushi
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society for Cell Biology 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4436784/
https://ncbi.nlm.nih.gov/pubmed/25717185
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E14-08-1287
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