Abstract
This protocol provides specific details on how to perform Chromatin immunoprecipitation (ChIP) from Drosophila embryos. ChIP allows the matching of proteins or histone modifications to specific genomic regions. Formaldehyde-cross-linked chromatin is isolated and antibodies against the target of interest are used to determine whether the target is associated with a specific DNA sequence. This can be performed in spatial and temporal manner and it can provide information about the genome-wide localization of a given protein or histone modification if coupled with deep sequencing technology (ChIP-Seq).
The original version of this chapter was revised. The erratum to this chapter is available at: DOI 10.1007/978-1-4939-6380-5_28
An erratum to this chapter can be found at http://dx.doi.org/10.1007/978-1-4939-6380-5_28
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Löser, E., Latreille, D., Iovino, N. (2016). Chromatin Preparation and Chromatin Immuno-precipitation from Drosophila Embryos. In: Lanzuolo, C., Bodega, B. (eds) Polycomb Group Proteins. Methods in Molecular Biology, vol 1480. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-6380-5_3
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DOI: https://doi.org/10.1007/978-1-4939-6380-5_3
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Publisher Name: Humana Press, New York, NY
Print ISBN: 978-1-4939-6378-2
Online ISBN: 978-1-4939-6380-5
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