Abstract
n -Propyl gallate (0.1 to 0.25 molar, in glycerol) reduces by a factor of 10 the rate of fading of fluorescence of cell structures labeled with tetramethylrhodamine or fluorescein-conjugated antibodies. Hence, prolonged photographic exposure of immunofluorescently labeled cells in the fluorescence microscope yields images with increased sensitivity, making feasible multiple data collection, as with serial optical sectioning.
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Dates
Type | When |
---|---|
Created | 18 years, 11 months ago (Oct. 5, 2006, 2:30 p.m.) |
Deposited | 1 year, 7 months ago (Jan. 14, 2024, 5:56 p.m.) |
Indexed | 2 days, 2 hours ago (Sept. 4, 2025, 9:14 a.m.) |
Issued | 42 years, 11 months ago (Sept. 24, 1982) |
Published | 42 years, 11 months ago (Sept. 24, 1982) |
Published Print | 42 years, 11 months ago (Sept. 24, 1982) |
@article{Giloh_1982, title={Fluorescence Microscopy: Reduced Photobleaching of Rhodamine and Fluorescein Protein Conjugates by n -Propyl Gallate}, volume={217}, ISSN={1095-9203}, url={http://dx.doi.org/10.1126/science.7112126}, DOI={10.1126/science.7112126}, number={4566}, journal={Science}, publisher={American Association for the Advancement of Science (AAAS)}, author={Giloh, Haim and Sedat, John W.}, year={1982}, month=sep, pages={1252–1255} }