Abstract
Mutant p53 may activate target genes through the interaction of transcription factors or through histone modifications. Chromatin immunoprecipitation (ChIP) is a method commonly used to study these types of protein interactions. In order to generate a list of target genes that may be activated through this mechanism, ChIP sequencing may be used. ChIP sequencing involves the mass parallel sequencing of ChIP DNA fragments. We describe a method by which to prepare chromatin immunoprecipitation sequencing libraries and how to analyze sequencing data. In this procedure, prepared libraries have been sent to a core facility. The results have been verified using quantitative PCR.
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© 2013 Springer Science+Business Media New York
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Vaughan, C., Windle, B., Deb, S. (2013). ChIP Sequencing to Identify p53 Targets. In: Deb, S., Deb, S. (eds) p53 Protocols. Methods in Molecular Biology, vol 962. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-236-0_19
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DOI: https://doi.org/10.1007/978-1-62703-236-0_19
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Publisher Name: Humana Press, Totowa, NJ
Print ISBN: 978-1-62703-235-3
Online ISBN: 978-1-62703-236-0
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