WB
Western blot analysis of lysates from HeLa cells using Acetyl-Histone H4-K12 Rabbit mAb at 1:1000 dilution incubated overnight at 4℃. HeLa cells were treated with TSA (1 μM) at 37℃ for 18 hours after serum starvation overnight.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.
Lysates/proteins: 30 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit.
Exposure time: 10 s.
WB
Western blot analysis of lysates from C6 cells using Acetyl-Histone H4-K12 Rabbit mAb at 1:1000 dilution incubated overnight at 4℃. C6 cells were treated with TSA (1 μM) at 37℃ for 18 hours after serum starvation overnight.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 30 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit .
Exposure time: 10 s.
IHC
Immunohistochemistry analysis of paraffin-embedded Human colon using Acetyl-Histone H4-K12 Rabbit mAb at dilution of 1:800 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate buffer (pH 6.0) prior to IHC staining.
IHC
Immunohistochemistry analysis of paraffin-embedded Mouse spleen using Acetyl-Histone H4-K12 Rabbit mAb at dilution of 1:800 (40x lens). High pressure antigen retrieval performed with 0.01M Citrate buffer (pH 6.0) prior to IHC staining.
IP
Immunoprecipitation analysis of 600 μg extracts of HeLa cells using 5 μg Acetyl-Histone H4-K12 Rabbit mAb. Western blot was performed from the immunoprecipitate using Acetyl-Histone H4-K5 Rabbit mAb at a dilition of 1:10000.
CHIP
Chromatin immunoprecipitation analysis of extracts of Hela cells, using Acetyl-Histone H4-K12 antibody and rabbit IgG.The amount of immunoprecipitated DNA was checked by quantitative PCR. Histogram was constructed by the ratios of the immunoprecipitated DNA to the input.