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. 2021 Feb 1;320(3):F485–F491. doi: 10.1152/ajprenal.00536.2020

Figure 1.

Figure 1.

Western blots of γENaC expressed in FRT cells. A: cells were transfected with WT γENaC together with αENaC and βENaC, with or without CAP1. Each pair of lanes represents a different transfection. Each lane was loaded with 10 µL of lysate from a different filter. CAP1 increased the abundance of a cleaved form of the subunit migrating at ∼65 kDa (white arrows) and decreased the intensities of the full-length species (black arrows) and of a diffuse band migrating around 75 kDa (gray arrows). The narrow band below 60 kDa is nonspecific, as it was also observed in nontransfected cells (right lane). B: densitometry of 80 kDa, 75 kDA, and 65 kDa bands from the blots in (A). Data were normalized in the absence of CAP1 and represent means ± SE; n = 4. **P < 0.01 vs. control by a paired two-tailed t test. CAP1, channel activating protease 1; ENaC, epithelial Na channel; FRT, Fisher rat thyroid; WT, wild-type.