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PMID: 2062120 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

High time resolution fluorescence imaging with a CCD camera.

Journal of neuroscience methods ·Vol. 36 ·No. 2-3 ·1991-02-00 ·Pages 253-61

Lasser-Ross N, Miyakawa H, Lev-Ram V, Young SR, Ross WN

Abstract

We have built a high speed, sensitive camera system capable of capturing sequences of low-light level images synchronized with recordings of membrane potential. The camera system is based on a cooled, scientific grade CCD camera controlled by a PC/AT computer. It can take 100 frames/sec of 18 X 18 element images and 40 frames/sec of 50 X 50 element images with no lag in response to step changes in light intensity. High accuracy and dynamic range of the measurements result from the fact that light levels of the picture elements are digitized with 12 bit accuracy with intrinsic camera noise levels typically less than 1/10,000 of the maximum detectable light level. We have used this system to record calcium dependent fura-2 fluorescence transients in the dendrites of cerebellar Purkinje cells and from different regions of leech neurons in segmental ganglia or isolated in culture.

MeSH Terms
Animals Calcium/metabolism Cerebellum/anatomy & histology,metabolism Dendrites/ultrastructure Diagnostic Imaging/instrumentation Electrodes Fluorescence Fura-2 Ganglia, Spinal/ultrastructure Leeches Membrane Potentials/physiology Photography Purkinje Cells/metabolism
Chemicals
Calcium Fura-2
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Lasser-Ross N
Department of Physiology, New York Medical College, Valhalla 10595.
Miyakawa H
Lev-Ram V
Young S R
Ross W N
Article Info
Journal
Journal of neuroscience methods
Abbr.
J Neurosci Methods
ISSN
0165-0270
Published
1991-02-00
Pages
253-61
Language
English
Region
Netherlands
NLM ID
7905558
Subset
IM
Grants
NINDS NIH HHS · R01 NS016295 · United States
NINDS NIH HHS · NS16295 · United States
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