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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]

Theyre small chains of amino acids that signal your body when its time to repair, recover, build muscle, or support healthy hormone function

This simple modification costs nothing and takes effect immediately