Chromatin immunoprecipitation (ChIP) is a method used to determine the location of DNA binding sites on the genome for a particular protein of interest. This technique gives a picture of the protein-DNA interactions that occur inside the nucleus of living cells or tissues. Determining how proteins interact with DNA to regulate gene expression is essential for fully understanding many biological processes and disease states.
Step-by-Step Guide to ChIP-Seq Sample Prep Products
All Next Generation Sequencing Platforms
Magnify™ Chromatin Immunoprecipitation System
Faster and more reproducible solution for Chromatin Immunoprecipitation (ChIP) with the ability to start with lower cell numbers to preserve precious samples.
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SOLiD® Applications
SOLiD® ChIP-Seq Kits
Complete & optimized system for genome wide Chromatin Immunoprecipitation (ChIP) analysis on SOLiD®. (Magnify™ ChIP System not required)
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SOLiD® Applications
SOLiD® Library TaqMan® Quantitation Kit
Enables measurement of amplifiable template in a SOLiD® library for optimal input in emulsion PCR (ePCR).
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SOLiD® Applications
SOLiD® Fragment Library Barcoding Kits
Unique barcode sequences for SOLiD® fragment libraries to sequence multiple samples on one slide. Increase throughput and efficiency while cutting cost.
Learn more
All Next Generation Sequencing Platforms
Magnify™ Chromatin Immunoprecipitation System
Faster and more reproducible solution for Chromatin Immunoprecipitation (ChIP) with the ability to start with lower cell numbers to preserve precious samples.
Learn more
SOLiD® Applications
SOLiD® ChIP-Seq Kits
Complete & optimized system for genome wide Chromatin Immunoprecipitation (ChIP) analysis on SOLiD®. (Magnify™ ChIP System not required)
Learn more
SOLiD® Applications
SOLiD® Library TaqMan® Quantitation Kit
Enables measurement of amplifiable template in a SOLiD® library for optimal input in emulsion PCR (ePCR).
Learn more
SOLiD® Applications
SOLiD® Fragment Library Barcoding Kits
Unique barcode sequences for SOLiD® fragment libraries to sequence multiple samples on one slide. Increase throughput and efficiency while cutting cost.
Learn more
NGS Resources
NGS Support
Next-Generation Sequencing Support Center
Find tips, troubleshooting help, and resources for your next-generation sequencing applications.
For Research Use Only. Not for use in diagnostic procedures.