| Literature DB >> 24215639 |
Benjamin Flottmann1, Manuel Gunkel, Tautvydas Lisauskas, Mike Heilemann, Vytaute Starkuviene, Jürgen Reymann, Holger Erfle.
Abstract
High-throughput microscopy is an effective tool for rapidly collecting data on a large scale. However, high throughput comes at the cost of low spatial resolution. Here we introduce correlative light microscopy by combining fast automated widefield imaging, confocal microscopy and super-resolution microscopy. We demonstrate the potential of this approach for scalable experiments. The workflow consists of a robust approach for selecting cells of interest on a wide-field screening microscope at low resolution and subsequently re-localizing those cells with micrometer precision for confocal and super-resolution imaging. As a case study, we visualized and quantified cis- and trans-Golgi markers at increasing resolution.Mesh:
Year: 2013 PMID: 24215639 DOI: 10.2144/000114099
Source DB: PubMed Journal: Biotechniques ISSN: 0736-6205 Impact factor: 1.993