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• W90394039 abstract "Live-cell imaging requires not only high temporal resolution but also illumination powers low enough to minimize photodamage. Traditional single-point laser scanning confocal microscopy (LSCM) is generally limited by both the relatively slow speed at which it can acquire optical sections by serial raster scanning (a few Hz) and the higher potential for phototoxicity. These limitations have driven the development of rapid, parallel forms of confocal microscopy, the most popular of which is the spinning-disk confocal microscope (SDCM). Here, we briefly introduce the SDCM technique, discuss its strengths and weaknesses against LSCM, and update the reader on some recent developments in SDCM technology that improve its performance and expand its utility for life science research now and in the future." @default.
• W90394039 created "2016-06-24" @default.
• W90394039 creator A5007995519 @default.
• W90394039 creator A5032520587 @default.
• W90394039 creator A5084066833 @default.
• W90394039 date "2014-01-01" @default.
• W90394039 modified "2023-10-01" @default.
• W90394039 title "Spinning-disk confocal microscopy" @default.
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• W90394039 doi "https://doi.org/10.1016/b978-0-12-420138-5.00009-4" @default.
• W90394039 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24974027" @default.
• W90394039 hasPublicationYear "2014" @default.
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