| Literature DB >> 26436332 |
Hilmar Strickfaden1, Zhi Zhong Xu2, Michael J Hendzel2.
Abstract
The limits to optical resolution and the challenge of identifying specific protein populations in transmission electron microscopy have been obstacles in cell biology. Many phenomena cannot be explained by in vitro analysis in simplified systems and need additional structural information in situ, particularly in the range between 1 nm and 0.1 µm, in order to be fully understood. Here, electron spectroscopic imaging, a transmission electron microscopy technique that allows simultaneous mapping of the distribution of proteins and nucleic acids, and an expression tag, miniSOG, are combined to study the structure and organization of DNA double-strand break repair foci.Mesh:
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Year: 2015 PMID: 26436332 PMCID: PMC4692621 DOI: 10.3791/52893
Source DB: PubMed Journal: J Vis Exp ISSN: 1940-087X Impact factor: 1.355