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PMID: 9674155 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Continuous wave excitation two-photon fluorescence microscopy exemplified with the 647-nm ArKr laser line.

Journal of microscopy ·Vol. 190 ·No. Pt 3 ·1998-06-00 ·Pages 298-304

Booth MJ, Hell SW

Abstract

We report on efficient two-photon fluorescence imaging in beam scanning microscopy by exciting UV dyes at the 647-nm line of a continuous wave ArKr mixed gas laser. For a numerical aperture of 1.4 (oil), we used an illumination power of up to 210 mW at the sample. High-resolution images were obtained for DAPI-labelled cell nuclei within 4-60 s. Our method is a simple two-photon alternative to UV confocal imaging with the potential of becoming a very useful feature of laser scanning microscopy.

MeSH Terms
Animals DNA/analysis Drosophila Fibroblasts Indoles Lasers Mice Microscopy, Confocal/instrumentation Microscopy, Fluorescence/instrumentation Photons
Chemicals
Indoles DAPI DNA
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Booth M J
High Resolution Optical Microscopy Group, Max-Planck-Institute for Biophysical Chemistry, Göttingen, Germany.
Hell S W
Article Info
Journal
Journal of microscopy
Abbr.
J Microsc
ISSN
0022-2720
Published
1998-06-00
Pages
298-304
Language
English
Region
England
NLM ID
0204522
Subset
IM
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