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In this study, we designed a peptide inhibitor based on the p53 transactivation domain (TAD) sequence and investigated its binding interface at the atomic level using NMR spectroscopy

Release it slowly against the vials inner wall to avoid foaming

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The most common experimental dose in animal studies (Sikiric et al.) is 10 g/kg/day intraperitoneally or orally in rats

Only report anatomical modifiers (-RT and -LT) if required by the payer, as incorrect usage may prompt a claim denial

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