EPG5 Polyclonal Antibody, 50ul[BT-AP15409] Pathway and Network Analysis |subunit:Composed of two components (A

|subunit:Composed of two components (A and B)| the A component is the catalytic subunit and the B component confers calcium sensitivity

and enhances cell transformation

Two different clinical disorders have been attributed to a defect of branched-chain amino acid transamination: hypervalinemia and hyperleucine-isoleucinemia

Mutations in this gene have been associated with Winchester syndrome and Nodulosis-Arthropathy-Osteolysis (NAO) syndrome

EPG5 Polyclonal Antibody, 50ul[BT-AP15409] Pathway and Network Analysis |subunit:Composed of two components (AThis gene encodes a large coiled coil domain containing protein that functions in autophagy during starvation conditions. Mutations in this gene cause Vici syndrome.