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Presented for research literature review only Lyon RP et al

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It should include: Batch number and lot code Testing methods (HPLC, mass spec, LAL endotoxin) Numeric results and acceptance criteria Analysts signature and date Look for at least 98% purity for clinical use

Because levels are often quite low before a deficiency is recognized, it can take some time for serum concentrations to even out and symptoms to subside

That stability profile is the main reason it appears so frequently in preclinical literature

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