AP2M1(Phospho-Thr156) Rabbit Polyclonal Antibody, 20ul Sample Library Tubes Mutation in this gene causes

Mutation in this gene causes dimethylglycine dehydrogenase deficiency

an octamer composed of pairs of each of the four core histones (H2A

antibody-dependent cell cytotoxicity

Calcium-activated potassium channel subunit beta-4 encoded by KCNMB4 is an auxiliary beta subunit which slows activation kinetics

AP2M1(Phospho-Thr156) Rabbit Polyclonal Antibody, 20ul Sample Library Tubes Mutation in this gene causesThis gene encodes a subunit of the heterotetrameric coat assembly protein complex 2 (AP2), which belongs to the adaptor complexes medium subunits family. The encoded protein is required for the activity of a vacuolar ATPase, which is responsible for proton pumping occurring in the acidification of endosomes and lysosomes. The encoded protein may also play an important role in regulating the intracellular trafficking and function of CTLA 4 protein.