| Literature DB >> 27592533 |
Kwasi Kwakwa1, Alexander Savell2,3, Timothy Davies4, Ian Munro2, Simona Parrinello4, Marco A Purbhoo5, Chris Dunsby2,6, Mark A A Neil2, Paul M W French2.
Abstract
TIRF and STORM microscopy are super-resolving fluorescence imaging modalities for which current implementations on standard microscopes can present significant complexity and cost. We present a straightforward and low-cost approach to implement STORM and TIRF taking advantage of multimode optical fibres and multimode diode lasers to provide the required excitation light. Combined with open source software and relatively simple protocols to prepare samples for STORM, including the use of Vectashield for non-TIRF imaging, this approach enables TIRF and STORM imaging of cells labelled with appropriate dyes or expressing suitable fluorescent proteins to become widely accessible at low cost.Entities:
Keywords: Microscopy; PALM; STORM; localization; super-resolution
Mesh:
Substances:
Year: 2016 PMID: 27592533 DOI: 10.1002/jbio.201500324
Source DB: PubMed Journal: J Biophotonics ISSN: 1864-063X Impact factor: 3.207