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Detection of specific chromosome structures by hybridization of fluorescence dye-conjugated probes to DNA. The FISH technique relies on the hybridization of DNA probes which identify specific chromosomal structures. Probes can be used which are specific for the centromere region of particular chromosomes, for genes, or for complete chromosomes. The DNA of both the applied probe and of the patient sample are denaturated, i.e., both DNA strands of the double helix are separated. During the following renaturation, the DNA probes attach to the complementary section of the patient’s DNA (hybridization). The DNA probes are either directly conjugated to a fluorescent dye or are analyzed using fluorescence conjugated antibodies. The respective chromosome structures therefore are assessable as fluorescence signals.
A significant advantage of the method lies in its applicability not only to metaphases but also to interphase nuclei. A disadvantage is that information is...
See Also
(2012) Centromere. In: Schwab M (ed) Encyclopedia of cancer, 3rd edn. Springer, Berlin/Heidelberg, p 744. doi: 10.1007/978-3-642-16483-5_1028
(2012) Chromosome. In: Schwab M (ed) Encyclopedia of cancer, 3rd edn. Springer, Berlin/ Heidelberg, p 848. doi: 10.1007/978-3-642-16483-5_1145
(2012) FISH. In: Schwab M (ed) Encyclopedia of cancer, 3rd edn. Springer, Berlin/Heidelberg, pp 1415–1416. doi: 10.1007/978-3-642-16483-5_2197
(2012) Fluorescence in situ hybridisation. In: Schwab M (ed) Encyclopedia of cancer, 3rd edn. Springer, Berlin/Heidelberg, p 1436. doi: 10.1007/978-3-642-16483-5_6740
(2012) PCR. In: Schwab M (ed) Encyclopedia of cancer, 3rd edn. Springer, Berlin/Heidelberg, p 2803. doi: 10.1007/978-3-642-16483-5_4417
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Schwab, M. (2015). Chromosomal Fluorescence In Situ Hybridization. In: Schwab, M. (eds) Encyclopedia of Cancer. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-27841-9_2218-2
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DOI: https://doi.org/10.1007/978-3-642-27841-9_2218-2
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Publisher Name: Springer, Berlin, Heidelberg
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