GST was immunoprecipitated in 0.2mg 293T-OE-GST cell lysate with ET1611-47 at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using ET1611-47 at 1/50,000 dilution. Anti-Rabbit IgG for IP Nano-secondary antibody (NBI01H) at 1/5,000 dilution was used for 1 hour at room temperature. Lane 1: 293T transfected with GST-tagged Histone H3.1 cell lysate (input) Lane 2: Rabbit IgG instead of ET1611-47 in 293T transfected with GST-tagged Histone H3.1 cell lysate Lane 3: ET1611-47 IP in 293T transfected with GST-tagged Histone H3.1 cell lysate Blocking/Dilution buffer: 5% NFDM/TBST Exposure time: 24 seconds

Immunocytochemistry analysis of HeLa transfected with GST-tagged Histone H3.1 cells labeling GST with Rabbit anti-GST antibody (ET1611-47) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-GST antibody (ET1611-47) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI. Histone H3 (HA601278, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.