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High-speed super resolution imaging of live fission yeast cells

We describe a step-by-step method for high-speed fluorescence photoactivation localization microscopy (FPALM) of live fission yeast cells. The resolution with this method is tenfold better than spinning disk confocal microscopy.

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Detaylı Bibliyografya
Yayımlandı:Methods Mol Biol
Asıl Yazarlar: Laplante, Caroline, Huang, Fang, Bewersdorf, Joerg, Pollard, Thomas D.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2016
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7319019/
https://ncbi.nlm.nih.gov/pubmed/26519304
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-1-4939-3145-3_4
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