A confocal setup to measure transmembrane potential in cardiac tissue with very high spatial and temporal resolution
We used a fast, fluorescent, potential sensitive indicator (di-4-ANEPPS) in combination with a specially designed setup which consists of an fluorescence microscope, a frequency doubled Nd:YAG laser and a 256 photodiode array system. The setup is especially designed to investigate tissue preparation...
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Published in: | Proceedings of the First Joint BMES/EMBS Conference : serving humanity advancing technology, Oct. 13-16, 99, Atlanta, GA, USA Vol. 1; pp. 164 vol.1 - 164 |
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Main Authors: | , , , , , |
Format: | Conference Proceeding Journal Article |
Language: | English |
Published: |
IEEE
1999
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Subjects: | |
Online Access: | Get full text |
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Summary: | We used a fast, fluorescent, potential sensitive indicator (di-4-ANEPPS) in combination with a specially designed setup which consists of an fluorescence microscope, a frequency doubled Nd:YAG laser and a 256 photodiode array system. The setup is especially designed to investigate tissue preparations in the mm range. The common setup can be reconstructed easily to a confocal laser microscope. This allows confocal microscopic detection of transmembrane potential with high temporal and spatial resolution. The axial resolution of the confocal results in a FWHM better then 15 /spl mu/m. Signals from papillary muscle were compared to images recorded by a CLSM (Leica TCS NT). |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-2 ObjectType-Feature-1 content type line 23 SourceType-Conference Papers & Proceedings-1 ObjectType-Conference-3 |
ISBN: | 0780356748 9780780356740 9780780356757 0780356756 |
ISSN: | 1094-687X 0589-1019 1558-4615 |
DOI: | 10.1109/IEMBS.1999.802209 |