Literature DB >> 8289227

A light-emitting diode light standard for photo- and videomicroscopy.

J M Beach1, B R Duling.   

Abstract

A light calibration system consisting of a compact light-emitting diode (LED) source with feedback control of intensity is described. The source is positioned in the focal plane of the microscope objective and produces flat-field illumination of up to 31 microW. The source can be easily used to determine the performance of microscope optics and camera response. It can also be used as a standard light source for calibration of experimental systems. Selectable light intensities are produced by controlling the LED input power via a feedback circuit consisting of a photodiode that detects output light intensity. Spectral coverage extends between 550 and 670 nm using green, yellow and red LEDs mounted side by side, which are selected individually. The LED chips are encapsulated in plastic diffusers which homogenize the light, and a flat field of illumination is obtained through a thin 1-mm-diameter aperture positioned directly over each chip. Provision is made for insertion of Ronchi rulings over the aperture to enable measurements of contrast modulation in a uniform field. The light may be pulse-modulated to assess camera response times and the device can be synchronized with video frames. Narrow bandpass interference filters can be placed between the objective lens and the LED source to produce monochromatic light without affecting the spacing of controlled light intensities since emission spectra do not shift appreciably over the range of LED powers chosen in this design. Results of tests using controlled light intensity and uniform illumination are presented.

Mesh:

Year:  1993        PMID: 8289227     DOI: 10.1111/j.1365-2818.1993.tb03391.x

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  2 in total

1.  Fluorescence emission spectral shift measurements of membrane potential in single cells.

Authors:  W Y Kao; C E Davis; Y I Kim; J M Beach
Journal:  Biophys J       Date:  2001-08       Impact factor: 4.033

2.  A novel optical microscope for imaging large embryos and tissue volumes with sub-cellular resolution throughout.

Authors:  Gail McConnell; Johanna Trägårdh; Rumelo Amor; John Dempster; Es Reid; William Bradshaw Amos
Journal:  Elife       Date:  2016-09-23       Impact factor: 8.140

  2 in total

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