ACM3 Polyclonal Antibody, 50ul Centrifuges Deficiency of this enzyme results

Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome)

This protein can interact with integrin-linked kinase (ILK/ILK1)

a disease characterized by hepatic dysfunction

and catalyzes the transfer of sulfate to position 4 of non-reducing N-acetylgalactosamine (GalNAc) residues in both N-glycans and O-glycans

The protein encoded by this gene binds to BTK and downregulates BTK's kinase activity

ACM3 Polyclonal Antibody, 50ul Centrifuges Deficiency of this enzyme resultsThe muscarinic cholinergic receptors belong to a larger family of G protein coupled receptors. The functional diversity of these receptors is defined by the binding of acetylcholine and includes cellular responses such as adenylate cyclase inhibition phosphoinositide degeneration and potassium channel mediation. Muscarinic receptors influence many effects of acetylcholine in the central and peripheral nervous system. The muscarinic cholinergic