| Literature DB >> 27514922 |
T Tony Yang1, Weng Man Chong1, Jung-Chi Liao2.
Abstract
The characteristic lengths of molecular arrangement in primary cilia are below the diffraction limit of light, challenging structural and functional studies of ciliary proteins. Superresolution microscopy can reach up to a 20 nm resolution, significantly improving the ability to map molecules in primary cilia. Here we describe detailed experimental procedure of STED microscopy imaging and dSTORM imaging, two of the most powerful superresolution imaging techniques. Specifically, we emphasize the use of these two methods on imaging proteins in primary cilia.Entities:
Keywords: Ciliary protein; Diffraction limit; Fluorophore; Primary cilium; STED; STORM; Superresolution microscopy
Mesh:
Year: 2016 PMID: 27514922 PMCID: PMC6865270 DOI: 10.1007/978-1-4939-3789-9_11
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745