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effects mediated mainly via ERR in cardiomyocytes

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The copper chelation capacity of AHK-Cu distinguishes it from unchelated peptide analogs, enabling research into coppers role as a cofactor in angiogenic and wound-response signaling

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The principle of using mAbs to increase IgG catabolism was also demonstrated in NHPs, when Nixon and colleagues at Dyax Corp used phage-display selected human IgG1 mAbs with high pH-independent affinity towards FcRn to reduce circulatory IgG without affecting albumin levels in NHPs [122]
