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Further, the ability of MeHg to inactivate GPx-1 at low nanomolar concentrations suggests that loss of GPx-1 activity may contribute to MeHg toxicity
Cell Cycle (2009) 8:153943
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If desired, cleavage of the protein from GST can be achieved using a site-specific protease whose recognition sequence is located immediately upstream from the multiple cloning site on the pGEX plasmids
A GHK-Cu solution that remains clear after reconstitution is a signal worth investigating before proceeding
Otherwise, it is not known whether a salt change or actually a new peptide derivative is being compared
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