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Ronsein GE, Pamir N, Von Haller PD, et al

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For the determination of the enzyme activity in a pH range of 6.07.0, the reaction mixture containing 50 mM 2-( N -morpholino)ethanesulfonic acid buffer, instead of 50 mM Tris-HCl buffer, was used

doi: 10.1158/1078-0432.CCR-13-1787 32 FrankenNARodermondHMStapJHavemanJvan BreeC

However, limited studies using murine models hint at a considerable anabolic potential of IGF-1 LR3

Once in solution, the peptide is no longer protected by the lyophilized matrix and becomes vulnerable to enzymatic degradation, oxidation, and thermal denaturation