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Article type: Review Article
Authors: Fritzky, Luke | Lagunoff, David
Affiliations: Core Imaging Facility, New Jersey Medical School, UM, NJ, USA
Note: [] Corresponding author: David Lagunoff, Adj. Professor, Department of Surgery, Director of Imaging Core Facility, Cancer Center, New Jersey Medical School, UM, NJ, USA. E-mail: [email protected]
Abstract: It requires a good deal of will power to resist hyperbole in considering the advances that have been achieved in fluorescence microscopy in the last 25 years. Our effort has been to survey the modalities of microscopic fluorescence imaging available to cell biologists and perhaps useful for diagnostic pathologists. The gamut extends from established confocal laser scanning through multiphoton and TIRF to the emerging technologies of super-resolution microscopy that breech the Abbé limit of resolution. Also considered are the recent innovations in structured and light sheet illumination, the use of FRET and molecular beacons that exploit specific characteristics of designer fluorescent proteins, fluorescence speckles, and second harmonic generation for native anisometric structures like collagen, microtubules and sarcomeres.
Keywords: Fluorescence microscopy, confocal microscopy, multiphoton microscopy, total internal reflectance microscopy (TIRFM), lateral sheet illumination microscopy, deconvolution, stimulated emission depletion microscopy (STED), reversible saturable/switchable optically linear fluorescence transition microscopy (RESOLFT), photoactivation localization microscopy (PALM), stochastic optical restoration microscopy (STORM), structured illumination microscopy (SIM), super-resolution optical fluctuation imaging (SOFI)
DOI: 10.3233/ACP-120071
Journal: Analytical Cellular Pathology, vol. 36, no. 1-2, pp. 5-17, 2013
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