Fig. 2From: Purification of functional mouse skeletal muscle mitochondria using percoll density gradient centrifugationBioenergetic profile of coupling assays in isolated mitochondria. (a) Determination of optimal mitochondrial input per well (1000, 500, 250 125 ng) in the presence of succinate/rotenone. (b) Absolute O2 tension (in mm Hg) in microchamber with different mitochondrial inputs. (c) Coupled mitochondrial respiration assays using 10 mM pyruvate/2 mm malate (PM), 10 mM glutamate/10 mM malate (GM), 40 μm palmitoyl L-carnitine/1 mM malate (PCM) and 10 mM succinate/2 uM rotenone (SR) as substrates with 600 ng mitochondrial input per well. (d) OCR for States 2, 3 4o and 3u and RCR for each of the substrates in (c). For Figures (a-c) data are expressed as pmol/min ± SEM or mm Hg ± SEM and in (d), as pmol/min ± SEM or the ratio of State 3/State 4o (RCR).Back to article page