Application
ELISA was performed using a serial dilution of CBFb antibody in antigen coated wells. By plotting the absorbance against the antibody dilution, the titer of the antibody was estimated to be 1:8,800.
Application
ChIP was performed with SKNO-1 nuclear extract and either 4 μl of CBFb antibody or control rabbit IgG. The precipitated DNA was detected by QPCR with primer set targeting to MYOG, FUT7, OGG1, NFE2 or SPI1.