Abstract
Chromatin immunoprecipitation followed by massively parallel sequencing (ChIP-Seq) is a powerful technique to map the genomic location of a given chromatin bound factor (i.e., transcription factors, cofactors) or epigenetic marks, such as histone modifi cation. The procedure is based on cross-linking of proteins to DNA followed by the capture of the protein-DNA complexes by “ChIP-grade” antibodies. In this chapter we describe in detail the experimental method developed in our laboratory to investigate in vivo the DNA- binding characteristics of a key heterodimeric nuclear receptor, the retinoid X receptor (RXR) in murine bone marrow-derived macrophages.
Original language | English (US) |
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Pages (from-to) | 15-24 |
Number of pages | 10 |
Journal | Methods in Molecular Biology |
Volume | 1204 |
DOIs | |
State | Published - 2014 |
Externally published | Yes |
Keywords
- Binding site
- ChIP
- Chromatin
- Cistrome
- Macrophage
- RXR
ASJC Scopus subject areas
- Molecular Biology
- Genetics