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Considering the fact that the activity of recombinant GPx3 from mammalian cells was similar to that of partially purified human plasma GPx3 18 , the significant drop in activity should be related to the absence of the post-translational modification

An unapproved, more-potent, IGFBP-resistant analog with no human safety data cannot be assumed to be safer, and by mechanism the same hazard categories are at least theoretically relevant

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It stopped acetylcholinesterase from working (IC 50 = 0.08 mM) (Xiao et al., 2002)

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aureus to antibiotics, without causing cytotoxicity or bacterial outgrowth