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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...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Biological Procedures Online
2005
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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. |
format | Text |
id | pubmed-1190380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Biological Procedures Online |
record_format | MEDLINE/PubMed |
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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