CUT & RUN Assay Kits
Cleavage Under Targets and Release Using Nuclease (CUT&RUN) is an advanced epigenomics technique designed to map protein-DNA interactions with high precision and minimal input requirements. This method utilizes antibody-directed targeting of a protein of interest, followed by enzymatic cleavage of DNA near binding sites. CUT&RUN is increasingly popular due to its sensitivity, simplicity, and reduced sequencing cost compared to traditional methods like ChIP-seq.
Content
- Principle of CUT&RUN
CUT&RUN combines the specificity of antibodies with the efficiency of enzymatic cleavage to profile protein-DNA interactions. The workflow involves:- Immobilization of cells or nuclei on a solid support.
- Antibody binding to the target protein of interest.
- Tethering of a Protein A/MNase fusion enzyme to the antibody.
- Controlled activation of MNase to cleave DNA proximal to the binding sites.
- Release of the cleaved DNA fragments for downstream sequencing.
- Key Features
- High sensitivity: Detects protein-DNA interactions from as few as 100–1,000 cells.
- Reduced sequencing depth: Enriched signal minimizes background noise.
- Compatibility: Works with diverse samples, including primary cells and tissues.
- Simplified workflow: Reduced experimental time and complexity.
Applications of CUT&RUN Assay Kits
CUT&RUN is widely used in molecular biology, epigenetics, and cancer research. Some of its specific applications include:
- Histone Modification Mapping: Identifying specific modifications like H3K27me3 or H3K4me3 to study chromatin states.
- Transcription Factor Studies: Determining binding sites of transcription factors such as CTCF, Oct4, or Sox2.
- Disease Research: Exploring epigenetic changes in diseases such as cancer, neurodegenerative disorders, and autoimmune conditions.
- Drug Discovery: Evaluating the impact of epigenetic drugs on protein-DNA interactions.
- Developmental Biology: Studying dynamic chromatin changes during development or differentiation.
CUT&RUN Assay Kits provide a robust and cost-effective solution for precise epigenomic studies, enabling researchers to explore complex gene regulatory mechanisms with high accuracy and efficiency.
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