Application
ChIP was performed with NIH3T3 extracts and 4 μg of pan-HP1 antibody. The precipitated DNA was detected by PCR with primers targeting to the rDNA promoter and a subtelomeric sequence of chromosome 19.
Application
WB analysis of nuclear extracts from HeLa cells (20 μg) using pan-HP1 antibody at a dilution of 1:1,000 in TBS-Tween containing 5% skimmed milk.
Application
ICC/IF analysis of HeLa cells using pan-HP1 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 labelled with pan-HP antibody at a dilution of 1:500.