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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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Bibliografische gegevens
Gepubliceerd in:Mol Biol Cell
Hoofdauteurs: Hayashi, Shinichi, Okada, Yasushi
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: The American Society for Cell Biology 2015
Onderwerpen:
Online toegang: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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