WB
Western blot analysis of lysates from HeLa cells, using MonoMethyl-Histone H3-K27 Rabbit mAb at1:30000 dilution.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.
Lysates/proteins: 25μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit.
Exposure time: 10s.
WB
Western blot analysis of various lysates, using MonoMethyl-Histone H3-K27 Rabbit mAb at1:30000 dilution.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.
Lysates/proteins: 25μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit.
Exposure time: 30s.
WB
Western blot analysis of lysates from Arabidopsis thaliana using MonoMethyl-Histone H3-K27 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: 60s.
DB
Dot-blot analysis of all sorts of peptides using MonoMethyl-Histone H3-K27 antibody at 1:30000 dilution.
ICC/IF
Confocal imaging of HeLa cells using MonoMethyl-Histone H3-K27 Rabbit mAb (dilution 1:100)(Red). The cells were counterstained with α-Tubulin Mouse mAb (dilution 1:400) (Green). DAPI was used for nuclear staining (blue). Objective: 100x.
ICC/IF
Immunofluorescence analysis of NIH/3T3 cells using MonoMethyl-Histone H3-K27 Rabbit mAb at dilution of 1:100(40x lens). Secondary antibody: Cy3-conjugated Goat anti-Rabbit IgG (H+L) at 1:500 dilution. Blue: DAPI for nuclear staining.