PPGB (20k, Cleaved-Met327) rabbit pAb - 50 μL

Catalytic activity: Release of a C-terminal amino acid with broad specificity. Disease: Defects in CTSA are the cause of galactosialidosis [MIM: 256540]. It is an autosomal recessive disease. function: Protective protein appears to be essential for both the activity of beta-galactosidase and neuraminidase, it associates with these enzymes and exerts a protective function necessary for their stability and activity. This protein is also a carboxypeptidase and can deamidate tachykinins. similarity: Belongs to the peptidase S10 family. subunit: Heterodimer of a 32 kDa chain and a 20 kDa chain; disulfide-linked.