WB
Western blot analysis of various lysates using Acetyl-Histone H4-K16 Rabbit mAb at 1:20000 dilution incubated overnight at 4℃. HeLa cells, NIH/3T3 cells and C6 cells were treated with TSA (1 uM) at 37℃ for 18 hours.
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.
DB
Dot-blot analysis of all sorts of peptides using Acetyl-Histone H4-K16 Rabbit mAb at 1:500 dilution.
IHC
Immunohistochemistry analysis of paraffin-embedded Moue pancreas tissue using Acetyl-Histone H4-K16 Rabbit mAb at a dilution of 1:5000 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer (pH 9.0) prior to IHC staining.
IHC
Immunohistochemistry analysis of paraffin-embedded Human colon tissue using Acetyl-Histone H4-K16 Rabbit mAb at a dilution of 1:5000 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer (pH 9.0) prior to IHC staining.
IHC
Immunohistochemistry analysis of paraffin-embedded Rat colon tissue using Acetyl-Histone H4-K16 Rabbit mAb at a dilution of 1:5000 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer (pH 9.0) prior to IHC staining.
CHIP
Chromatin immunoprecipitation analysis of extracts of HeLa cells, using Acetyl-Histone H4-K16 Rabbit mAb 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.