Desmin Polyclonal Antibody, 100ul[BT-AP02570] Enzyme Activity Assays AMPD3 encodes a member of

AMPD3 encodes a member of the AMP deaminase gene family

ADULT syndrome (acro-dermato-ungual-lacrim

and mutations in SCN4A have been linked to several myotonia and periodic paralysis disorders

This complex functions as an upstream activator of NF-kappaB signaling

Desmin Polyclonal Antibody, 100ul[BT-AP02570] Enzyme Activity Assays AMPD3 encodes a member ofDES encodes a muscle specific class III intermediate filament. Homopolymers of desmin form a stable intracytoplasmic filamentous network connecting myofibrils to each other and to the plasma membrane. Mutations in DES are associated with desmin related myopathy, a familial cardiac and skeletal myopathy (CSM), and with distal myopathies.