Mitochondrial pellet was resuspended in digitonin buffer (30 mM HEPES-KOH, pH 7.4, 150 mM potassium acetate, 10 [v/v] glycerol, and 1 mg of digitonin) and kept on ice for 30 min. Ten microliters of antibody serum, 50 mL of Protein A-Sepharose, 1 (w/v) BSA, and Complete protease inhibitor (Roche) were added to the mitochondria and incubated for 6 h at 4 on a rotating wheel at 20 rpm. Beads were

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Flanked by Gateway recombination cassettes (Supplemental Table S4) and cloned intoMurcha et al.pDONR201. LR reactions were carried out with C-terminal GFP fusion vectors for GFP localization (Carrie et al., 2009), pDEST14 for in vitro transcription and translation, and pB2GW7 (35S CaMV promoter) for Agrobacterium tumefaciensmediated complementation (Karimi et al., 2002). Yeast two-hybrid vectors w

Ver the age of 65. Interestingly, there is no significant difference between the non frail and frail groups of patients admitted to intensive care. This may be because of small sample size. The length of stay of the frail patient is shorter and this may be because as intensivists we are better at treatment limitation in this group of patients. No difference in overall mortality suggests that the p

Ver the age of 65. Interestingly, there is no significant difference between the non frail and frail groups of patients admitted to intensive care. This may be because of small sample size. The length of stay of the frail patient is shorter and this may be because as intensivists we are better at treatment limitation in this group of patients. No difference in overall mortality suggests that the p

Ver the age of 65. Interestingly, there is no significant difference between the non frail and frail groups of patients admitted to intensive care. This may be because of small sample size. The length of stay of the frail patient is shorter and this may be because as intensivists we are better at treatment limitation in this group of patients. No difference in overall mortality suggests that the p

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