Skip to main content
. 2008 Feb 15;22(4):528–542. doi: 10.1101/gad.463208

Figure 5.

Figure 5.

Epistasis analysis of Trabid’s function in the Wnt pathway. TOPFLASH assays in 293T cells transfected with siRNAs as in Figure 4F and cotransfected with empty vector, HA-Wnt3A (A), stabilized Flag-β-catenin (Δ45S) (B), or 50–100 ng of catC-LEF1Δ56 or 1–5 ng VP16-LEF1ΔN chimeras (C), as indicated (the expression levels of the two chimeras were chosen to result in comparable transactivation). (Below) Western blots from a representative experiment to monitor expression levels of endogenous or overexpressed proteins (α-β-catenin antibody was used to detect catC-LEF1Δ56; VP16-LEF1ΔN was undetectable at these low expression levels); numbers below the blot in C indicate relative levels of catC-LEF1Δ56 expression (normalized to lane 2).