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Even fluorescence excitation by multidirectional selective plane illumination microscopy (mSPIM)

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Huisken, Jan, Stainier, Didier Y. R.·2007·Optics Letters

Abstract

Multidirectional selective plane illumination microscopy (mSPIM) reduces absorption and scattering artifacts and provides an evenly illuminated focal plane. mSPIM solves two common problems in light-sheet-based imaging techniques: The shadowing in the excitation path due to absorption in the specimen is eliminated by pivoting the light sheet; the spread of the light sheet by scattering in the sample is compensated by illuminating the sample consecutively from opposing directions. The resulting two images are computationally fused yielding a superior image. The effective light sheet is thinner, and the axial resolution is increased by square root 2 over single-directional SPIM. The multidirectional illumination proves essential in biological specimens such as millimeter-sized embryos. The performance of mSPIM is demonstrated by the imaging of live zebrafish embryos.

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Metadata

Authors
Huisken, J., & Stainier, D. Y. R.
Venue
Optics Letters
Published
2007-08-27
Volume
32
Issue
17
Pages
2608
ISSN
  • 0146-9592 (ISSN-L)
  • 1539-4794
OpenAlex
W2110021835
Cited by
424
References
0
FWCI
4.95
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Even fluorescence excitation by multidirectional selective plane illumination microscopy (mSPIM). https://app.cochat.ai/papers/10.1364/ol.32.002608
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Huisken, J., & Stainier, D. Y. R. (2007). Even fluorescence excitation by multidirectional selective plane illumination microscopy (mSPIM). Optics Letters. https://doi.org/10.1364/ol.32.002608

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