Application
ChIP was performed with the nuclear extract of mouse macrophage (derived from bone marrow) and either 1 μg of PPARG antibody or control rabbit IgG. The precipitated DNA was detected by QPCR with primer set targeting to PDK4 PPAR response element (RE).
Application
WB analysis of 293T cells transfected with pNTAP-PPARG (lane 1) and non-transfected cells (lane 2) using PPARG antibody diluted 1:2,000 in TBS-Tween containing 3% skimmed milk.
Application
ELISA was performed using a serial dilution of PPARG antibody in antigen coated wells. By plotting the absorbance against the antibody dilution, the titer of the antibody was estimated to be 1:70,250.