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Related Concept Videos

Chromatin Immunoprecipitation- ChIP02:36

Chromatin Immunoprecipitation- ChIP

Chromatin immunoprecipitation, or ChIP, is an antibody-based technique used to identify sites on DNA that bind to transcription factors of interest or histone proteins. It also helps determine the type of histone modifications such as acetylation, phosphorylation, or methylation.
Types of ChIP
ChIP can be divided into two types - X-ChIP and N-ChIP. X-ChIP involves in vivo cross-linking of histones and regulatory proteins to DNA, fragmenting the DNA by sonication, and isolating the protein-DNA...
Immunoprecipitation01:20

Immunoprecipitation

Immunoprecipitation, or IP, is a widely used technique that employs protein-antibody interactions to isolate proteins or protein complexes in their native state for studying protein-protein interactions, quaternary structures, or supramolecular complexes. Various modifications of the technique, including chromatin IP, cross-linking IP, and fluorescence IP, are commonly used.
Chromatin Immunoprecipitation
Chromatin immunoprecipitation, also known as ChIP, is used to study protein-DNA or...

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Related Experiment Video

Updated: Jun 21, 2026

Chromatin Immunoprecipitation (ChIP) Protocol for Low-abundance Embryonic Samples
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Published on: August 29, 2017

MicroChIP: chromatin immunoprecipitation for small cell numbers.

John Arne Dahl1, Philippe Collas

  • 1Department of Biochemistry, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.

Methods in Molecular Biology (Clifton, N.J.)
|July 10, 2009
PubMed
Summary

This study introduces a rapid micro (micro)ChIP assay for analyzing protein-DNA interactions using minimal cell numbers. This fast chromatin immunoprecipitation technique enables multiple parallel assays from just 1,000 cells.

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Area of Science:

  • Molecular Biology
  • Genomics
  • Epigenetics

Background:

  • Chromatin immunoprecipitation (ChIP) is crucial for studying protein-DNA interactions and mapping histone modifications.
  • Conventional ChIP requires large cell numbers, limiting its use with rare cell samples.
  • Existing ChIP assays for small cell numbers are often time-consuming.

Purpose of the Study:

  • To develop a fast and efficient ChIP assay for small cell populations.
  • To enable multiple parallel ChIP analyses from a single chromatin batch.
  • To optimize ChIP for immunoprecipitating histone proteins and transcription factors.

Main Methods:

  • Development of a rapid micro (micro)ChIP assay.
  • Application to small cell numbers ranging from 100 to 100,000 cells.
  • Performed under cross-linking conditions for histone proteins and transcription factors.

Main Results:

  • The microChIP assay is suitable for multiple parallel ChIPs from 1,000 cells.
  • A single immunoprecipitation can be performed using as few as 100 cells.
  • The assay significantly reduces the time and cell input required for ChIP.

Conclusions:

  • The rapid microChIP assay provides a streamlined method for studying protein-DNA interactions in limited cell samples.
  • This technique expands the applicability of ChIP to rare cell types and small-scale experiments.
  • The assay facilitates high-throughput epigenomic studies with reduced sample requirements.