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Conversion of a Peroxiredoxin into a Disulfide Reductase by a Triplet Repeat Expansion

Once concentration is known, every dose is just target mcg divided by mcg per mL

Next, the apo-enzyme was eluted using GST elution buffer (50 mM Tris, 10 mM methylglutathione, pH 8) before relevant fractions were combined according to their A 280nm