CUTANA™ pAG-MNase for ChIC/CUT&RUN Workflows – 50 Reactions
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- 50 Reactions
- 250 Reactions
45 in stock
Powered by Bioz- Type: Nuclease
- Mol Wgt: 43.7 kDa
- Host: E. coli
- Epitope Tag: 6xHis
Available in 50 and 250 Reaction pack sizes. CUTANA™ pAG-MNase is the key reagent for performing Chromatin Immunocleavage (ChIC) [Schmid et al., 2004] and Cleavage Under Targets and Release Using Nuclease (CUT&RUN) [Skene & Henikoff, 2017, Skene et al., 2018].
As a fusion of Proteins A and G to Micrococcal Nuclease, CUTANA pAG-MNase is compatible with target antibodies from a broad spectrum of host species and is highly purified to remove contaminating E. coli DNA, which can complicate analysis at low cell numbers. This enzyme enables efficient mapping of chromatin features in ChIC/CUT&RUN, allowing for significant improvements in signal to noise at reduced cell inputs and sequencing depth compared to ChIP-seq.
Figure 1: CUT&RUN gene browser tracks
CUT&RUN was performed as described above. Data verifies low non-specific MNase digestion with the absence of peaks in the IgG track, an expected H3K4me3 profile with sharp promoter peaks, and broad peaks in heterochromatin regions consistent with H3K27me3. Image was generated using the Integrative Genomics Viewer (IGV, Broad Institute).
Figure 2: Size distribution of released chromatin
CUT&RUN was performed as described above. Excised DNA is highly enriched for mononucleosomes (peaks at ~300 bp represent 150 bp nucleosomes + sequencing adapters).
Figure 3: CUT&RUN genome-wide heatmaps
CUT&RUN was performed as described above. Heatmaps show CUT&RUN signal aligned to annotated transcription start sites (TSS, +/- 2kb). High and low signal are ranked by intensity (top to bottom) and colored such that red indicates high localized enrichment and blue denotes background signal. Gene rows in each heatmap are aligned and sorted from high to low signal relative to H3K4me3 (middle).
Figure 4: Protein gel data
CUTANA™ pAG-MNase (1 µg) was resolved via SDS-PAGE and stained with Coomassie blue. The migration and molecular weight of the protein standards are indicated.
CUT&RUN methods
CUT&RUN was performed on 500k K562 cells with 0.5 µg of either IgG (EpiCypher 13-0042), H3K4me3 (EpiCypher 13-0041), or H3K27me3 (ThermoFisher MA5-11198) antibodies using CUTANA™ pAG-MNase (1:20 dilution) and the CUTANA™ ChIC/CUT&RUN Kit v3 (EpiCypher 14-1048). Library preparation was performed with 5 ng of DNA (or the total amount recovered if less than 5 ng) using the CUTANA™ CUT&RUN Library Prep Kit (EpiCypher 14-1001/14-1002). Both kit protocols were adapted for high throughput Tecan liquid handling. Libraries were run on an Illumina NextSeq2000 with paired-end sequencing (2×50 bp). Sample sequencing depth was 3.6 million reads (IgG), 4.3 million reads (H3K4me3), and 5.2 million reads (H3K27me3). Data were aligned to the hg19 genome using Bowtie2. Data were filtered to remove duplicates, multi-aligned reads, and ENCODE DAC Exclusion List regions.