Application
Fig1: Western blot analysis of Histone H3 (mono methyl K18) on HepG2 cell lysates with Rabbit anti-Histone H3 (mono methyl K18) antibody at 1/500 dilution.
Lysates/proteins at 10 µg/Lane.
Exposure time: 2 minutes;
15% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody at 1/500 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.
Application
Fig2: Western blot analysis of Histone H3 (mono methyl K18) on mouse testis tissue lysates with Rabbit anti-Histone H3 (mono methyl K18) antibody at 1/5,000 dilution.
Lysates/proteins at 20 µg/Lane.
Exposure time: 1 minute;
15% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody at 1/5,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody at 1:300,000 dilution was used for 1 hour at room temperature.
Application
Fig3: ICC staining Histone H3(mono methyl K18) in PC-3M cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Application
Fig4: ICC staining Histone H3(mono methyl K18) in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
Application
Fig5: Immunohistochemical analysis of paraffin-embedded mouse testis tissue using anti-Histone H3(mono methyl K18) antibody. Counter stained with hematoxylin.
Application
Fig6: Immunohistochemical analysis of paraffin-embedded mouse kidney tissue using anti-Histone H3(mono methyl K18) antibody. Counter stained with hematoxylin.