Liver phospho-eEF2 (A), representative phospho-Thr-56-eEF2 and eEF2 western blots (B) and protein synthesis rate (C) in goldfish exposed to normoxia (N;∼

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Supplementary data d a c d ab b Figure S1. Quantification of the Western blot data in figure 4C. The area density of each band was measured with a UVP.

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Presentation transcript:

Liver phospho-eEF2 (A), representative phospho-Thr-56-eEF2 and eEF2 western blots (B) and protein synthesis rate (C) in goldfish exposed to normoxia (N;∼ 9.5 mg O2l–1; open squares) and 12 h of hypoxia (∼0.3 mg O2l–1; closed squares). Liver phospho-eEF2 (A), representative phospho-Thr-56-eEF2 and eEF2 western blots (B) and protein synthesis rate (C) in goldfish exposed to normoxia (N;∼ 9.5 mg O2l–1; open squares) and 12 h of hypoxia (∼0.3 mg O2l–1; closed squares). Horizontal broken lines through normoxia are shown as a reference. Bands shown on representative western blot are at ∼95 kDa. Data are means ± s.e.m. (N=5 to 8). *Significant difference from normoxia, P<0.05. Lindsay A. Jibb, and Jeffrey G. Richards J Exp Biol 2008;211:3111-3122 © The Company of Biologists Limited 2008