| Literature DB >> 34331287 |
Raja Chouket1, Ruikang Zhang1, Agnès Pellissier-Tanon1, Annie Lemarchand2, Agathe Espagne1, Thomas Le Saux3, Ludovic Jullien4.
Abstract
Fluorescence imaging has become a powerful tool for observations in biology. Yet it has also encountered limitations to overcome optical interferences of ambient light, autofluorescence, and spectrally interfering fluorophores. In this account, we first examine the current approaches which address these limitations. Then we more specifically report on Out-of-Phase Imaging after Optical Modulation (OPIOM), which has proved attractive for highly selective multiplexed fluorescence imaging even under adverse optical conditions. After exposing the OPIOM principle, we detail the protocols for successful OPIOM implementation.Keywords: Dynamic contrast; Fluorescence endomicroscopy; Fluorescence imaging; Fluorescence microscopy; Macroscale imaging; Reversibly photoswitchable fluorophores
Year: 2021 PMID: 34331287 DOI: 10.1007/978-1-0716-1593-5_13
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745