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. 2015 Oct 29;4:e06011. doi: 10.7554/eLife.06011

Figure 5. PDZ-RhoGEF is required for optimal IGF-1 signaling output in EWAT.

(A) IR phosphorylation and differential PKB/Akt phosphorylation in WT and PDZ-RhoGEF KO EWAT in response to insulin. (B) Serine phosphorylation of IRS1 and interaction between IRS1 and PI3K in WT and PDZ-RhoGEF KO EWAT in response to insulin. (C) IR phosphorylation and differential PKB/Akt phosphorylation in WT and PDZ-RhoGEF KO liver in response to insulin. (D) IR phosphorylation and differential PKB/Akt phosphorylation in WT and PDZ-RhoGEF KO skeletal muscle in response to insulin.

DOI: http://dx.doi.org/10.7554/eLife.06011.018

Figure 5.

Figure 5—figure supplement 1. The tissue expression profile of PDZ-RhoGEF.

Figure 5—figure supplement 1.

The indicated tissue lysates were immunoblotted with the anti-PDZ-RhoGEF antibody.