WB
Western blot analysis of lysates from C6 cells using Symmetric DiMethyl-Histone H4-R3 Rabbit mAb at 1:1000 dilution incubated overnight at 4℃.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.
Lysates/proteins: 25 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit.
Exposure time: 10s.
DB
Dot-blot analysis of H3R2me0、H3R2me1、H3R2me2a、H3R2me2s、H3R8me0、H3R8me1、H3R8me2a、H3R8me2s、H3R17me0、H3R17me1、H3R17me2a、H3R17me2s、H3R26me0、H3R26me1、H3R26me2a、H3R26me2s、H4R3me0、H4R3me1、H4R3me2a、H4R3me2s peptides using Symmetric DiMethyl-Histone H4-R3 Rabbit mAb at 1:1000 dilution.
ICC/IF
Confocal imaging of U-2 OS cells using Symmetric DiMethyl-Histone H4-R3 Rabbit mAb (dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (dilution 1:500) (Red). The cells were counterstained with α-Tubulin Mouse mAb (dilution 1:400) followed by incubation with 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.