Literature DB >> 21052173

Quantitative comparison of background rejection, signal-to-noise ratio, and resolution in confocal and full-field laser scanning microscopes.

D R Sandison, D W Piston, R M Williams, W W Webb.   

Abstract

Development of a laser scanning microscope for simultaneous three-dimensional imaging in both a full-field laser scanning mode (FLSM) and a confocal laser scanning mode (CLSM) permits the direct comparison of axial resolution and out-of-focus background rejection as a function of sample thickness for both FLSM and CLSM with varying detector aperture (pinhole) radii. The sample-dependent detector aperture radii that optimize the signal-to-noise ratio (S/N) in the CLSM are experimentally determined. The results verify earlier calculations [Appl. Opt. 33, 603 (1994)]. Using these results, we discuss the practical and theoretical limits on the S/N in the CLSM and compare them with those of a full-field epifluorescence microscope (FEM) that is enhanced by image deconvolution. The specimen volume over which the FLSM exhibits imaging properties that are equivalent to a FEM is calculated in the appendices.

Year:  1995        PMID: 21052173     DOI: 10.1364/AO.34.003576

Source DB:  PubMed          Journal:  Appl Opt        ISSN: 1559-128X            Impact factor:   1.980


  13 in total

1.  True optical resolution beyond the Rayleigh limit achieved by standing wave illumination.

Authors:  J T Frohn; H F Knapp; A Stemmer
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-20       Impact factor: 11.205

2.  Measuring tubulin content in Toxoplasma gondii: a comparison of laser-scanning confocal and wide-field fluorescence microscopy.

Authors:  Jason R Swedlow; Ke Hu; Paul D Andrews; David S Roos; John M Murray
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-05       Impact factor: 11.205

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Authors:  Samuel T Hess; Thanu P K Girirajan; Michael D Mason
Journal:  Biophys J       Date:  2006-09-15       Impact factor: 4.033

4.  Electron microscopy of whole cells in liquid with nanometer resolution.

Authors:  N de Jonge; D B Peckys; G J Kremers; D W Piston
Journal:  Proc Natl Acad Sci U S A       Date:  2009-01-21       Impact factor: 11.205

Review 5.  Two-photon in vivo imaging of cells.

Authors:  Daniel J Christensen; Maiken Nedergaard
Journal:  Pediatr Nephrol       Date:  2011-03-15       Impact factor: 3.714

6.  Two-photon excitation improves multifocal structured illumination microscopy in thick scattering tissue.

Authors:  Maria Ingaramo; Andrew G York; Peter Wawrzusin; Oleg Milberg; Amy Hong; Roberto Weigert; Hari Shroff; George H Patterson
Journal:  Proc Natl Acad Sci U S A       Date:  2014-03-24       Impact factor: 11.205

7.  Glucose suppression of glucagon secretion: metabolic and calcium responses from alpha-cells in intact mouse pancreatic islets.

Authors:  Sylvain J Le Marchand; David W Piston
Journal:  J Biol Chem       Date:  2010-03-15       Impact factor: 5.157

8.  Versatile, do-it-yourself, low-cost spinning disk confocal microscope.

Authors:  Aaron R Halpern; Min Yen Lee; Marco D Howard; Marcus A Woodworth; Philip R Nicovich; Joshua C Vaughan
Journal:  Biomed Opt Express       Date:  2022-02-01       Impact factor: 3.732

9.  Quantitative evaluation of skeletal muscle defects in second harmonic generation images.

Authors:  Wenhua Liu; Nina Raben; Evelyn Ralston
Journal:  J Biomed Opt       Date:  2013-02       Impact factor: 3.170

10.  Ultrahigh resolution imaging of biomolecules by fluorescence photoactivation localization microscopy.

Authors:  Samuel T Hess; Travis J Gould; Mudalige Gunewardene; Joerg Bewersdorf; Michael D Mason
Journal:  Methods Mol Biol       Date:  2009
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