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ghk-cu copper binding affinity The difference between AHK-Cu and lies in their target specificity. Both use ions as an enzymatic cofactor, but their amino acid sequences determine their individual affinity. 𧬠GHK-Cu targets extracellular C-BrainCog
GHK-CU | Pantheon Peptides
As shown in Fig.6h, D-CuP exhibited significantly stronger binding affinities, with equilibrium dissociation constants (KD) of 3.8 Γ 10β»βΆ M for p53 and 1.81 Γ 10β»βΆ M for HDAC7
C-BrainCog
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