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Scanningless depth-resolved microscopy
Open accessAbstract
The ability to perform optical sectioning is one of the great advantages of laser-scanning microscopy. This introduces, however, a number of difficulties due to the scanning process, such as lower frame rates due to the serial acquisition process. Here we show that by introducing spatiotemporal pulse shaping techniques to multiphoton microscopy it is possible to obtain full-frame depth resolved imaging completely without scanning. Our method relies on temporal focusing of the illumination pulse. The pulsed excitation field is compressed as it propagates through the sample, reaching its shortest duration at the focal plane, before stretching again beyond it. This method is applied to obtain depth-resolved twophoton excitation fluorescence (TPEF) images of drosophila egg-chambers with nearly 105 effective pixels using a standard Ti:Sapphire laser oscillator.
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Cites
Highly Nonlinear Photodamage in Two-Photon Fluorescence Microscopy
Hopt, A., & Neher, E. (2001) · Biophysical Journal · doi:10.1016/s0006-3495(01)76173-5 · Cited by 442
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Metadata
- Authors
- Oron, D., Tal, E., & Silberberg, Y.
- Venue
- Optics Express
- Publisher
- Optica Publishing Group
- Published
- 2005-03-07
- Volume
- 13
- Issue
- 5
- Pages
- 1468
- ISSN
- 1094-4087 (ISSN-L)
- OpenAlex
- W1996353817
- Cited by
- 449
- References
- 1
- FWCI
- 6.01
- Type
- journal article
- Language
- en
- Open access
- gold
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