Application
Dot blot analysis of peptides containing histone modifications and the unmodified H3K18 using H3K18ac antibody at a dilution of 1:5,000. One hundred to 0.2 pmol of the respective peptides were spotted on a membrane for analysis.
Application
WB analysis of whole cell (25 μg, lane 1) and histone extracts (15 μg, lane 2) from HeLa cells, and 1 μg of recombinant histone H2A, H2B, H3 and H4 (lane 3, 4, 5 and 6, respectively) using H3K18ac antibody at a dilution of 1:500 in TBS-Tween containing 5% skimmed milk.
Application
ICC/IF analysis of HeLa cells using H3K18ac antibody (green) and DAPI (blue). Cells were fixed with 4% formaldehyde for 10’ and blocked with PBS/TX-100 containing 5% normal goat serum and 1% BSA. The cells were immunofluorescently labeled with H3K18ac antibody at a dilution of 1:200.
Application
ChIP was performed with extracts from TSA-treated HeLa cells and either control IgG (2 μg) or Histone H3K18ac (acetyl Lys18) antibody (1, 2, 5 and 10 μg per ChIP experiment). The precipitated DNA was detected by qPCR with primers targeting to positive controls c-fos and EIF4A2 promoters, and to negative controls MYOD1 gene and the Sat2 satellite repeat.
Application
ELISA was performed using a serial dilution of Histone H3K18ac (acetyl Lys18) antibody in antigen coated wells. By plotting the absorbance against the antibody dilution, the titer of the antibody was estimated to be 1:4,300