Kv1.3(Phospho Tyr187) Polyclonal Antibody, 50ul Cell Dissociation Mutations in ADAMTS2 cause Ehlers-Danlos

Mutations in ADAMTS2 cause Ehlers-Danlos syndrome type VIIC

resulting in the synthesis of G(M2) and G(D2)

and the expansion of these repeats from the normal 12-44 to 52-86 is one cause of Machado-Joseph disease

It is thought to play a role in T-cell proliferation and differentiation

The encoded transmembrane protein is a receptor for the soluble ligand ectodysplasin A

Kv1.3(Phospho Tyr187) Polyclonal Antibody, 50ul Cell Dissociation Mutations in ADAMTS2 cause Ehlers-DanlosPotassium channels represent the most complex class of voltage gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence related potassium channel genes shaker, shaw, shab, and shal have been identified in Drosophila, and each has