CD238 Polyclonal Antibody, 100ul Polyclonal Antibodies Mutations in this gene have

Mutations in this gene have been associated with thrombophilia due to protein C deficiency| neonatal purpura fulminans| and recurrent venous thrombosis

sometimes including retinal dystrophy and renal disease

and probably has a role in controlling the excitability of motor neurons

delta and epsilon

Ubiquitin carboxyl-terminal hydrolase isozyme L1 encoded by UCHL1 belongs to the peptidase C12 family

CD238 Polyclonal Antibody, 100ul Polyclonal Antibodies Mutations in this gene haveKEL (Kell blood group, metallo endopeptidase) encodes a type II transmembrane glycoprotein that is the highly polymorphic Kell blood group antigen. The Kell glycoprotein links via a single disulfide bond to the XK membrane protein that carries the Kx antigen. The encoded protein contains sequence and structural similarity to members of the neprilysin (M13) family of zinc endopeptidases.