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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...

詳細記述

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書誌詳細
出版年:Mol Biol Cell
主要な著者: Hayashi, Shinichi, Okada, Yasushi
フォーマット: Artigo
言語:Inglês
出版事項: The American Society for Cell Biology 2015
主題:
オンライン・アクセス: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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