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Updated: May 2, 2026

Simultaneous Multicolor Imaging of Biological Structures with Fluorescence Photoactivation Localization Microscopy
Published on: December 10, 2013
Protocol for 3D sub-10-nm multicolor expansion STED nanoscopy using small-molecule organic probes
Jing Yan1, Yubing Han1, Xiang Hao1
1State Key Laboratory of Extreme Photonics and Instrumentation, College of Optical Science and Engineering, Zhejiang University, Hangzhou 310027, China.
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Expansion microscopy (ExM) physically enlarges specimens, enhancing resolution. Here, we present a protocol for integrating small-molecule organic probes (SMOPs) and adaptive optics (AO) into expansion stimulated emission depletion (ExSTED) microscopy to achieve sub-10-nm resolution at depths of 10-50 μm in biological specimens. We describe steps for probe design and synthesis, cell labeling, multicolor staining, and cell expansion. We detail procedures for AO-corrected stimulated emission depletion (STED) imaging workflow. This protocol applies to high-resolution 3D imaging of cellular and tissue structures. For complete details on the use and execution of this protocol, please refer to Han et al.1 and Tu et al.2.

