| Literature DB >> 30324598 |
Carmina Angelica Perez-Romero1,2, Huy Tran1,3, Mathieu Coppey4, Aleksandra M Walczak3, Cécile Fradin1,2, Nathalie Dostatni5.
Abstract
Live imaging has been used in recent years for the understanding of dynamic processes in biology, such as embryo development. This was made possible by a combination of advancements in microscopy, leading to improved signal-to-noise ratios and better spatial and temporal resolutions, and by the development of new fluorescence markers, allowing for the quantification of protein expression and transcriptional dynamics in vivo. Here we describe a general protocol, which can be used in standard confocal microscopes to image early Drosophila melanogaster embryos, in order to learn about the transcriptional dynamics of a fluorescently labeled RNA.Entities:
Keywords: Confocal microscopy; Embryo; Live imaging; MS2 system; RNA
Mesh:
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Year: 2018 PMID: 30324598 DOI: 10.1007/978-1-4939-8772-6_10
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745