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Related Experiment Video

Updated: Jun 3, 2026

Method for the Isolation and Identification of mRNAs, microRNAs and Protein Components of Ribonucleoprotein Complexes from Cell Extracts using RIP-Chip
13:34

Method for the Isolation and Identification of mRNAs, microRNAs and Protein Components of Ribonucleoprotein Complexes from Cell Extracts using RIP-Chip

Published on: September 29, 2012

RNA-binding protein immunopurification-microarray (RIP-Chip) analysis to profile localized RNAs.

Alessia Galgano1, André P Gerber

  • 1Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, ETH Zurich, Zurich, Switzerland.

Methods in Molecular Biology (Clifton, N.J.)
|March 25, 2011
PubMed
Summary
This summary is machine-generated.

RNA-binding proteins (RBPs) control gene expression post-transcriptionally. This protocol details RNA-binding protein immunopurification-microarray profiling (RIP-Chip) for identifying RBP-bound mRNAs genome-wide.

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Identification of Footprints of RNA:Protein Complexes via RNA Immunoprecipitation in Tandem Followed by Sequencing (RIPiT-Seq)

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Method for the Isolation and Identification of mRNAs, microRNAs and Protein Components of Ribonucleoprotein Complexes from Cell Extracts using RIP-Chip
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Identification of Footprints of RNA:Protein Complexes via RNA Immunoprecipitation in Tandem Followed by Sequencing (RIPiT-Seq)
09:26

Identification of Footprints of RNA:Protein Complexes via RNA Immunoprecipitation in Tandem Followed by Sequencing (RIPiT-Seq)

Published on: July 10, 2019

Area of Science:

  • Molecular Biology
  • Genetics
  • Biochemistry

Background:

  • Post-transcriptional gene regulation is essential for cellular function.
  • RNA-binding proteins (RBPs) play a critical role in modulating mRNA expression.
  • Understanding RBP-mRNA interactions is key to deciphering gene regulatory networks.

Purpose of the Study:

  • To provide a detailed protocol for genome-wide identification of mRNA targets of RBPs.
  • To introduce RNA-binding protein immunopurification-microarray profiling (RIP-Chip) as a systematic method.
  • To highlight the utility of RIP-Chip in studying RBP-RNA networks and their dynamics.

Main Methods:

  • Purification of endogenous RBP-mRNA complexes using specific antibodies.
  • Identification of associated RNAs via DNA microarrays (RIP-Chip).
  • Application of RIP-Chip to study mRNA transport and subcellular localization.

Main Results:

  • The RIP-Chip method enables systematic examination of RNA targets for RBPs.
  • This technique allows for the genome-wide identification of mRNAs regulated by specific RBPs.
  • RIP-Chip can identify mRNAs transported by RNP-motor complexes to specific cellular compartments.

Conclusions:

  • RIP-Chip is a powerful technique for dissecting post-transcriptional gene regulation.
  • Further development of this method can offer global insights into RBP-RNA networks.
  • Understanding these networks is crucial for comprehending cellular processes, development, and disease.