Supplementary Figure 3: The expressed fusion proteins did not exhibit notable degradation.
From: Spatial orchestration of mitochondrial translation and OXPHOS complex assembly
Shown are Western Blots of whole cell extracts decorated with an antiserum against GFP, as indicated. As a loading control of each western blot, a porin specific serum was used. Outlines indicate different exposure times that were used to ensure optimal signal to noise ratios for proteins with different expression levels on the same blot. All experiments were repeated at least two times with similar results. The full blots are shown in Supplementary Figure 6
