Literature DB >> 18536650

A rapid micro chromatin immunoprecipitation assay (microChIP).

John Arne Dahl1, Philippe Collas.   

Abstract

Interactions of proteins with DNA mediate many critical nuclear functions. Chromatin immunoprecipitation (ChIP) is a robust technique for studying protein-DNA interactions. Current ChIP assays, however, either require large cell numbers, which prevent their application to rare cell samples or small-tissue biopsies, or involve lengthy procedures. We describe here a 1-day micro ChIP (microChIP) protocol suitable for up to eight parallel histone and/or transcription factor immunoprecipitations from a single batch of 1,000 cells. MicroChIP technique is also suitable for monitoring the association of one protein with multiple genomic sites in 100 cells. Alterations in cross-linking and chromatin preparation steps also make microChIP applicable to approximately 1-mm(3) fresh- or frozen-tissue biopsies. From cell fixation to PCR-ready DNA, the procedure takes approximately 8 h for 16 ChIPs.

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Year:  2008        PMID: 18536650     DOI: 10.1038/nprot.2008.68

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   13.491


  141 in total

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Journal:  Nat Protoc       Date:  2011-09-29       Impact factor: 13.491

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7.  Chromatin immunoprecipitation and gene expression analysis of neuronal subtypes after fluorescence activated cell sorting.

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Journal:  J Neurosci Methods       Date:  2016-02-08       Impact factor: 2.390

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Journal:  Genes Dev       Date:  2011-02-01       Impact factor: 11.361

9.  Broad histone H3K4me3 domains in mouse oocytes modulate maternal-to-zygotic transition.

Authors:  John Arne Dahl; Inkyung Jung; Håvard Aanes; Gareth D Greggains; Adeel Manaf; Mads Lerdrup; Guoqiang Li; Samantha Kuan; Bin Li; Ah Young Lee; Sebastian Preissl; Ingunn Jermstad; Mads Haugland Haugen; Rajikala Suganthan; Magnar Bjørås; Klaus Hansen; Knut Tomas Dalen; Peter Fedorcsak; Bing Ren; Arne Klungland
Journal:  Nature       Date:  2016-09-14       Impact factor: 49.962

10.  DNA hypermethylation in prostate cancer is a consequence of aberrant epithelial differentiation and hyperproliferation.

Authors:  D Pellacani; D Kestoras; A P Droop; F M Frame; P A Berry; M G Lawrence; M J Stower; M S Simms; V M Mann; A T Collins; G P Risbridger; N J Maitland
Journal:  Cell Death Differ       Date:  2014-01-24       Impact factor: 15.828

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