Abstract
When combined with molecular analysis and immunocytological localization, fluorescence in situ hybridization (FISH) represents one of the most direct and precise experimental tools in current biological research (1-4). Direct visualization and in situ detection fill the gap between molecular analysis and cytological description and provide a new avenue for in vitro and in vivo comparison. Such a system facilitates the understanding of cellular events not only with respect to what and how, but also where and when.
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Heng, H.H.Q. (2000). Released Chromatin or DNA Fiber Preparations for High-Resolution Fiber FISH. In: Darby, I.A. (eds) In Situ Hybridization Protocols. Methods in Molecular Biology™, vol 123. Humana Press. https://doi.org/10.1385/1-59259-677-0:69
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DOI: https://doi.org/10.1385/1-59259-677-0:69
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Print ISBN: 978-0-89603-686-4
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