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To ensure optimal FcRn binding, cellular transport, and PK properties of albumin-based biologics, we attempted to substitute the C-terminal L585 of albumin with an amino acid residue that would not be recognized by CPA
Rapid increases or self-adjustment raises risks of adverse effects, medication interactions, and improper technique
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Oxidized roGFP2 WT , PfGrx C88S , and PfGrx C32S/C88S were produced by incubation of the reduced enzymes with 5 mM Diamide for 60 min on ice
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