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Easy detection of chromatin binding proteins by the histone association assay

The Histone Association Assay provides an easy approach for detecting proteins that bind chromatin in vivo. This technique is based on a chromatin immunoprecipitation protocol using histone H3-specific antibodies to precipitate bulk chromatin from crosslinked whole cell extracts. Proteins that co-pr...

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Detalles Bibliográficos
Autores principales: Ricke, Robin, Bielinsky, Anja-Katrin
Formato: Texto
Lenguaje:English
Publicado: Biological Procedures Online 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1190380/
https://www.ncbi.nlm.nih.gov/pubmed/16136225
http://dx.doi.org/10.1251/bpo106
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author Ricke, Robin
Bielinsky, Anja-Katrin
author_facet Ricke, Robin
Bielinsky, Anja-Katrin
author_sort Ricke, Robin
collection PubMed
description The Histone Association Assay provides an easy approach for detecting proteins that bind chromatin in vivo. This technique is based on a chromatin immunoprecipitation protocol using histone H3-specific antibodies to precipitate bulk chromatin from crosslinked whole cell extracts. Proteins that co-precipitate with chromatin are subsequently detected by conventional SDS-PAGE and Western blot analysis. Unlike techniques that separate chromatin and non-chromatin interacting proteins by centrifugation, this method can be used to delineate whether a protein is chromatin associated regardless of its innate solubility. Moreover, the relative amount of protein bound to DNA can be ascertained under quantitative conditions. Therefore, this technique may be utilized for analyzing the chromatin association of proteins involved in diverse cellular processes.
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spelling pubmed-11903802005-08-31 Easy detection of chromatin binding proteins by the histone association assay Ricke, Robin Bielinsky, Anja-Katrin Biol Proced Online Research Article The Histone Association Assay provides an easy approach for detecting proteins that bind chromatin in vivo. This technique is based on a chromatin immunoprecipitation protocol using histone H3-specific antibodies to precipitate bulk chromatin from crosslinked whole cell extracts. Proteins that co-precipitate with chromatin are subsequently detected by conventional SDS-PAGE and Western blot analysis. Unlike techniques that separate chromatin and non-chromatin interacting proteins by centrifugation, this method can be used to delineate whether a protein is chromatin associated regardless of its innate solubility. Moreover, the relative amount of protein bound to DNA can be ascertained under quantitative conditions. Therefore, this technique may be utilized for analyzing the chromatin association of proteins involved in diverse cellular processes. Biological Procedures Online 2005-05-09 /pmc/articles/PMC1190380/ /pubmed/16136225 http://dx.doi.org/10.1251/bpo106 Text en Copyright © May 05, 2005, R Ricke et al. This paper is Open Access and is published in Biological Procedures Online under license from the authors. Copying, printing, redistribution and storage permitted.
spellingShingle Research Article
Ricke, Robin
Bielinsky, Anja-Katrin
Easy detection of chromatin binding proteins by the histone association assay
title Easy detection of chromatin binding proteins by the histone association assay
title_full Easy detection of chromatin binding proteins by the histone association assay
title_fullStr Easy detection of chromatin binding proteins by the histone association assay
title_full_unstemmed Easy detection of chromatin binding proteins by the histone association assay
title_short Easy detection of chromatin binding proteins by the histone association assay
title_sort easy detection of chromatin binding proteins by the histone association assay
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1190380/
https://www.ncbi.nlm.nih.gov/pubmed/16136225
http://dx.doi.org/10.1251/bpo106
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