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Description

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Clinical Trial Activity References Quality & Purity This product is synthesized via solid-phase peptide synthesis (SPPS) and tested to 99% purity by HPLC with identity confirmed by mass spectrometry

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Researchers who have used 1mL of bacteriostatic water for reconstituting the 5mg vial will have to withdraw 50U via an U-100 insulin syringe to initiate their experiments with 2.5mg/weekly

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