Differential destabilization of repetitive sequence hybrids in fluorescence in situ hybridization

A method for painting a chromosome or chromosome region by fluorescence in situ hybridization (FISH) without blocking DNA is described. Both unique sequence and repetitive sequence components of a fluorescently labeled probe are hybridized under low-stringency conditions, but the chromosomes are was...

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Veröffentlicht in:Cytogenetic and genome research 1998-01, Vol.83 (1-2), p.60-63
Hauptverfasser: Hozier, J.C., Scalzi, J.M., Clase, A.C., Davis, L.M., Liechty, M.C.
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Sprache:eng
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Zusammenfassung:A method for painting a chromosome or chromosome region by fluorescence in situ hybridization (FISH) without blocking DNA is described. Both unique sequence and repetitive sequence components of a fluorescently labeled probe are hybridized under low-stringency conditions, but the chromosomes are washed in such a manner that repetitive sequences are differentially removed, while region-specific unique sequence fragments remain bound to the target chromosomes. We refer to this differential retention and removal of probe components as differential stability FISH.
ISSN:1424-8581
0301-0171
1424-859X
DOI:10.1159/000015127