Whole cell extract (30 μg) was separated by 10% SDS-PAGE, and the membrane was blotted with FVT1 antibody [N2C3] (GTX119050) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.