Application
ChIP was performed with SKNO-1 nuclear extract and either 4 μl of ETO antibody or control rabbit IgG. The precipitated DNA was detected by QPCR with primer set targeting to H2B, OGG1, FUT7, NFE2 or VEGF.
Application
ELISA was performed using a serial dilution of ETO / RUNX1T1 antibody in antigen coated wells. By plotting the absorbance against the antibody dilution, the titer of the antibody was estimated to be 1:1,300.