Micro chromatin immunoprecipitation (μChIP) from early mammalian embryos

4Citations
Citations of this article
14Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Chromatin immunoprecipitation (ChIP) is a powerful method for mapping protein-DNA interactions in vivo. Genomic localization of histone modifications, transcription factors, and other regulatory proteins can be revealed by ChIP. However, conventional ChIP protocols require the use of large numbers of cells, which prevents the application of ChIP to rare cell types. We have developed ChIP assays suited for the immunoprecipitation of histone proteins or transcription factors from small cell numbers. Here we describe a rapid, yet sensitive micro (μ)ChIP protocol producing high signal to noise ratio output, suitable for as few as 100 cells. This chapter provides a detailed protocol for μChIP from early mammalian embryos, also suitable for any sample of limited numbers of cells. Minor modifications of this optimized high signal to noise ChIP protocol make it a reliable tool for the use with any cell number (100-10(7)).

Cite

CITATION STYLE

APA

Dahl, J. A. rne, & Klungland, A. (2015). Micro chromatin immunoprecipitation (μChIP) from early mammalian embryos. Methods in Molecular Biology (Clifton, N.J.), 1222, 227–245. https://doi.org/10.1007/978-1-4939-1594-1_17

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free