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Cited by 2,355

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Optical Sectioning Deep Inside Live Embryos by Selective Plane Illumination Microscopy

Huisken, Jan, Swoger, Jim, Del Bene, Filippo, Wittbrodt, Joachim, Stelzer, Ernst H. K.·2004·Science

Abstract

Large, living biological specimens present challenges to existing optical imaging techniques because of their absorptive and scattering properties. We developed selective plane illumination microscopy (SPIM) to generate multidimensional images of samples up to a few millimeters in size. The system combines two-dimensional illumination with orthogonal camera-based detection to achieve high-resolution, optically sectioned imaging throughout the sample, with minimal photodamage and at speeds capable of capturing transient biological phenomena. We used SPIM to visualize all muscles in vivo in the transgenic Medaka line Arnie, which expresses green fluorescent protein in muscle tissue. We also demonstrate that SPIM can be applied to visualize the embryogenesis of the relatively opaque Drosophila melanogaster in vivo.

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Metadata

Authors
Huisken, J., Swoger, J., Del Bene, F., Wittbrodt, J., & Stelzer, E. H. K.
Venue
Science
Published
2004-08-13
Volume
305
Issue
5686
Pages
1007-1009
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2030224529
Cited by
2,355
References
0
FWCI
14.32
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Optical Sectioning Deep Inside Live Embryos by Selective Plane Illumination Microscopy. https://app.cochat.ai/papers/10.1126/science.1100035
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Huisken, J., Swoger, J., Del Bene, F., Wittbrodt, J., & Stelzer, E. H. K. (2004). Optical Sectioning Deep Inside Live Embryos by Selective Plane Illumination Microscopy. Science. https://doi.org/10.1126/science.1100035

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