| Literature DB >> 27631997 |
Kasey J Day1, Effrosyni Papanikou1, Benjamin S Glick2.
Abstract
Yeast cells are well suited to visualizing organelles by 4D confocal microscopy. Typically, one or more cellular compartments are labeled with a fluorescent protein or dye, and a stack of confocal sections spanning the entire cell volume is captured every few seconds. Under appropriate conditions, organelle dynamics can be observed for many minutes with only limited photobleaching. Images are captured at a relatively low signal-to-noise ratio and are subsequently processed to generate movies that can be analyzed and quantified. Here, we describe methods for acquiring and processing 4D data using conventional scanning confocal microscopy.Entities:
Keywords: 4D microscopy; Confocal; Deconvolution; ImageJ; Photobleaching; Yeast
Mesh:
Year: 2016 PMID: 27631997 PMCID: PMC5086802 DOI: 10.1007/978-1-4939-6463-5_1
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745