Literature DB >> 18312724

Light-emitting diodes are better illumination sources for biological microscopy than conventional sources.

Richard W Cole1, James N Turner.   

Abstract

Light-emitting diodes (LEDs) can be easily and inexpensively integrated into modern light microscopes. There are numerous advantages of LEDs as illumination sources; most notably, they provide brightness and spectral control. We demonstrate that for transmitted light imaging, an LED can replace the traditional tungsten filament bulb while offering longer life; no color temperature change with intensity change; reduced emission in the infrared region, which is important for live cell imaging; and reduced cost of ownership. We show a direct substitution of the typical tungsten bulb with a commercially available LED and demonstrated the color stability by imaging a histology section over a wide range of light intensities. For fluorescent imaging, where the typical illumination sources are mercury or xenon lamps, we demonstrate that LEDs offer advantages of providing a longer lifespan, having a more constant intensity output over time, more homogeneous illumination, and significantly lower photon dose. Our LED equipped system was used to image and deconvolve dual fluorescently labeled cells, as well as image cells undergoing mitosis expressing green fluorescent protein-histone 2B complex. The timing of the stages of mitosis is well established as an indicator of cell viability.

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Year:  2008        PMID: 18312724     DOI: 10.1017/S1431927608080288

Source DB:  PubMed          Journal:  Microsc Microanal        ISSN: 1431-9276            Impact factor:   4.127


  8 in total

1.  Measuring and interpreting point spread functions to determine confocal microscope resolution and ensure quality control.

Authors:  Richard W Cole; Tushare Jinadasa; Claire M Brown
Journal:  Nat Protoc       Date:  2011-11-10       Impact factor: 13.491

2.  A systematic study on fluorescence enhancement under single-photon pulsed illumination.

Authors:  Arijit Kumar De; Debabrata Goswami
Journal:  J Fluoresc       Date:  2009-06-09       Impact factor: 2.217

3.  Live-cell imaging.

Authors:  Richard Cole
Journal:  Cell Adh Migr       Date:  2014-10-31       Impact factor: 3.405

4.  Epi-fluorescence microscopy.

Authors:  Donna J Webb; Claire M Brown
Journal:  Methods Mol Biol       Date:  2013

5.  Mercury free microscopy: an opportunity for core facility directors.

Authors:  T Regan Baird; Daniel Kaufman; Claire M Brown
Journal:  J Biomol Tech       Date:  2014-07

6.  Light-induced Ca(2+) transients observed in widefield epi-fluorescence microscopy of excitable cells.

Authors:  Alison McDonald; John Harris; Debbi Macmillan; John Dempster; Gail McConnell
Journal:  Biomed Opt Express       Date:  2012-05-04       Impact factor: 3.732

Review 7.  Recent Advances in Luminescence Imaging of Biological Systems Using Lanthanide(III) Luminescent Complexes.

Authors:  Jorge H S K Monteiro
Journal:  Molecules       Date:  2020-04-29       Impact factor: 4.411

8.  Open LED Illuminator: A Simple and Inexpensive LED Illuminator for Fast Multicolor Particle Tracking in Neurons.

Authors:  Jens B Bosse; Nikhila S Tanneti; Ian B Hogue; Lynn W Enquist
Journal:  PLoS One       Date:  2015-11-23       Impact factor: 3.240

  8 in total

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