CUTANA Multiomic CUT&RUN Assays

CUTANA™ Multiomic CUT&RUN Assays

Next-Gen Multiomic Profiling of DNA Methylation and Chromatin Proteins

Rich Insights with a Streamlined, Cost-Effective Approach

Traditional multiomic DNA methylation approaches integrate chromatin immunoprecipitation sequencing (ChIP-seq) with whole-genome bisulfite sequencing (WGBS) datasets. However, these assays are cost-prohibitive for many labs, require large numbers of cells, and take weeks (or longer!) to complete. Moreover, simply overlaying ChIP-seq and WGBS datasets cannot directly capture how chromatin proteins and DNA methylation functionally interact at the same loci, limiting the biological insights that can be derived.

Multiomic CUT&RUN allows you to see the full picture of chromatin regulation with a single workflow!

A Breakthrough Approach for DNA Methylation Research

CUTANA™ Multiomic CUT&RUN is the first workflow to enable simultaneous detection of DNA methylation and chromatin proteins in a single reaction. 

Figure 1: The CUTANA™ Multiomic CUT&RUN workflow can be divided into 3 easy steps. In Step 1, CUT&RUN is used to enrich target-bound chromatin. Only 5,000-500,000 cells per reaction is needed. In Step 2, unmethylated cytosines are converted to uracils for base-pair resolution DNA methylation analysis. Note that enzymatic or bisulfite conversion may be used. Step 3 is next-generation sequencing and data analysis. Only 30-50 M total reads are needed for robust multiomic analysis of target protein and underlying DNA methylation.

Explore DNA Methylation + Histone PTM
and Chromatin Protein Crosstalk

Powered by CUT&RUN technology, this approach provides base-pair resolution of CpG methylation at transcription factor binding sites, histone PTMs, and chromatin-modifying enzymes (Figure 2).

Key observations:

  • No 5mC at active promoters marked by H3K4me3
  • High association of 5mC with H3K36me3, a PTM that denotes active gene bodies and intergenic regions
  • Transcription factors generally have low tolerance for DNA methylation (e.g. CTCF)
Do more with less—sample, time, and budget. Extract maximum data from minimal input, reducing both sequencing needs and experimental complexity.

Multiomic CUT&RUN is compatible with various cell lines and sample types (Figure 3), and requires just 30-50 M total sequencing reads, making it ideal for studying:

  • Cancer epigenetics: Transposon reactivation and biomarker discovery
  • Developmental regulation: Transcriptional silencing and heterochromatin dynamics
  • Genomic stability: Chromatin structure response to drugs, environment, toxins

Figure 3: Multiomic CUT&RUN with EM-seq conversion (CUT&RUN-EM) reveals levels of CpG methylation associated with distinct chromatin proteins, across various cells lines. Black dots represent replicates.

Get Started with CUTANA Multiomic CUT&RUN Today!

We have everything you need to get started with Multiomic CUT&RUN:

  • Multiomic CUT&RUN Controls Set: The key postitive and negative controls for Multiomic CUT&RUN, plus our expert guidance via a new workflow manual!
  • CUT&RUN Kit A user-friendly kit to enrich target chromatin; key for Multiomic CUT&RUN assays.
  • CUT&RUN-Validated Antibodies High quality antibodies with exquisite sensitivity, expertly validated for CUT&RUN.
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