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Updated: Aug 1, 2025

Using Light Sheet Fluorescence Microscopy to Image Zebrafish Eye Development
Published on: April 10, 2016
TissUExM protocol for ultrastructure expansion microscopy of zebrafish larvae and mouse embryos
Emmanuelle Steib1, Christina Vagena-Pantoula1, Julien Vermot1
1Department of Bioengineering, Imperial College London, London SW7 2AZ, UK.
Abstract:
Expansion microscopy of millimeter-large mechanically heterogeneous tissues, such as whole vertebrate embryos, has been limited, particularly when combined with post-expansion immunofluorescence. Here, we present a protocol to perform ultrastructure expansion microscopy of whole vertebrate embryos, optimized to perform post-expansion labeling. We describe steps for embedding and denaturing zebrafish larvae or mouse embryos. We then detail procedures for hydrogel handling and mounting. This protocol is particularly well suited for super-resolution imaging of macromolecular protein complexes in situ but does not preserve lipids. For complete details on the use and execution of this protocol, please refer to Steib et al.1.
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