Application
ChIP was performed with U2OS nuclear extract and 1.5 μg of MBD1 antibody. Beads only were used as a negative IP control. The precipitated DNA was detected by QPCR with primer set targeting to GAPDH promoter or myoglobin.
Application
WB analysis of nuclear extracts (40 μg) of HeLa cells using MBD1 antibody diluted 1:500 in TBS-Tween containing 5% skimmed milk.
Application
ELISA was performed using a serial dilution of MBD1 antibody in antigen coated wells. By plotting the absorbance against the antibody dilution, the titer of the purified antibody was estimated to be 1:20,000.