| Literature DB >> 25271962 |
Laura Furia1, Piergiuseppe Pelicci, Mario Faretta.
Abstract
Optical fluorescence microscopy offers a wide range of technological solutions to address many questions in biomedical research. Spatial resolution has been greatly improved by the use of confocal microscopes, providing a 3-D analysis of the intracellular space. Automation has contributed to make confocal analysis available for high-content image cytometry studies. However, the storage, browsing, and analysis of the amount of data generated can challenge the feasibility of such studies. Presented in this chapter is a multistep acquisition and analysis protocol that can bypass such difficulties by an analysis-driven data collection. Cell-cycle analysis of low-resolution data can be employed to select cell populations of interest that can then be imaged at extremely high resolution and subjected to high-content analysis.Keywords: S phase; automated microscopy; cell cycle; confocal microscopy; high content; high resolution; image cytometry
Mesh:
Year: 2014 PMID: 25271962 DOI: 10.1002/0471142956.cy0742s70
Source DB: PubMed Journal: Curr Protoc Cytom ISSN: 1934-9297