CUT&RUN was preformed as described in Figure   7. CUT&RUN sequencing reads were aligned to the unique DNA barcodes corresponding   to each nucleosome in the SNAP-CUTANA™ DYKDDDDK Tag Panel (EpiCypher 19-5001). Data are   expressed as a percent relative to on-target recovery (DYKDDDDK Tag set to   100%) or total counts (IgG/GATA3). IgG/GATA3 show no preferential binding to   unmodified or DYKDDDDK spike-in nucleosomes. DYKDDDDK Tag antibody   selectively enriches the DYKDDDDK Tag spike-in nucleosome, validating the   antibody in CUT&RUN.

Figure 2: DYKDDDDK-tagged protein peaks in CUT&RUN

CUT&RUN was preformed as described in Figure 7.   Heatmaps show DYKDDDDK Tag antibody-enriched peaks called for FLAG-GATA3   overexpressing cells (OE) in aligned rows relative to all other experimental   conditions. Rows are ranked by intensity (top to bottom) and colored such   that red indicates high localized enrichment and blue denotes background   signal. A high degree of overlap is observed for DYKDDDDK and GATA3   antibodies as expected in the OE cells, while empty vector control (Ctrl)   shows absence of FLAG and lower GATA3 enrichment representing endogenous   protein. IgG shows low background signal. H3K4me3, a canonical mark of   promoters, does not appear in regions of high GATA3 enrichment.

Figure 3: CUT&RUN representative browser tracks for   DYKDDDDK-tagged protein

CUT&RUN was preformed as described in Figure 7.   Gene browser shots were generated using the Integrative Genomics Viewer (IGV,   Broad Institute). Two of the top called peaks in FLAG-GATA3 overexpressing   (OE) cells are shown. The peaks show the same distribution patterns as   observed in the genome-wide heatmaps (Figure 2). IgG shows low background,   H3K4me3 is unchanged between empty vector control (Ctrl) and OE cells, GATA3   peaks are more robust in OE cells, and peaks overlap between GATA3 and   DYKDDDDK antibodies in OE cells. These results demonstrate the robustness and   specificity of DYKDDDDK Tag antibody in CUT&RUN experiments targeting FLAG-tagged   proteins.

Figure 4: Western blot data

Western analysis of FLAG-tagged protein in lysates from   non-transfected human HEK293 cells, HEK293 transfected with Met-FLAG-IDO1,   HEK293 transfected with IDO1-FLAG-HIS (Internal Tag), HEK293 transfected with   IDO1-HIS-FLAG (C-Terminal Tag), and SUP-M2 cells. EpiCypher DYKDDDDK Tag   antibody was used at 1:1,000. An HRP-conjugated goat anti-rabbit IgG antibody   (Fortis A120-101P) was used as a secondary antibody. Chemiluminescence   exposure time was 10 seconds. Lower panel shows rabbit anti-RPS3A antibody   results (Fortis A305-003A).

Figure 5: Immunoprecipitation data

EpiCypher DYKDDDDK Tag antibody (20 µL/mg lysate) was   used to immunoprecipitate lysates isolated from HEK293 cells transfected with   either Met-FLAG-IDO1 (A) or IDO1-HIS-FLAG (C-terminal tag; B). For blotting   immunoprecipitated DYKDDDDK Tag, EpiCypher DYKDDDDK Tag antibody was used at   1:1,000. Chemiluminescence exposure time was 10 seconds.

Figure 6: Immunocytochemistry data

FFPE sections of HEK293 cells expressing either   FLAG-tagged nuclear protein (left) or FLAG-tagged cytoplasmic protein (right)   using EpiCypher DYKDDDDK Tag antibody. An HRP-conjugated goat anti-rabbit IgG   antibody (Fortis A120-501P) was used as a secondary antibody. The substrate   used was DAB.

Figure 7: CUT&RUN methods

CUT&RUN was performed on 500k MDA-MB-231 native   cells either stably overexpressing 3xFLAG-tagged GATA3 [1] or containing   vector control. Either DYKDDDDK Tag (0.05 µg), H3K4me3 (0.5 µg; EpiCypher   13-0041), GATA3 (0.5 µg; CST 5852), or IgG (0.5 µg, EpiCypher 13-0042)   antibodies were used with 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). Libraries were run on an Illumina   NextSeq2000 with paired-end sequencing (2x50 bp). Sample sequencing depth   (vector control cells/overexpressing cells) was 5.6/4.5 million reads (IgG),   7.8/6.7 million reads (H3K4me3), 5.8/4.7 million reads (GATA3), and 6.2/5.5   million reads (DYKDDDDK Tag). Data were aligned to the hg19 genome using   Bowtie2. Data were filtered to remove duplicates, multi-aligned reads, and   ENCODE DAC Exclusion List regions.

13-2031

DYKDDDDK Tag   CUTANA™ CUT&RUN Antibody

100 µL