ABCA8 Polyclonal Antibody, 50ul Cell Proliferation Deficiency of the muscle-specific enzyme

Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human

This protein binds IL13 with high affinity

The protein encoded by this gene is an inositol 1|4|5-trisphosphate (InsP3) 5-phosphatase and contains a Sac domain

This protein is a member of the trypsin family of peptidases

binding is inhibited by GTP

ABCA8 Polyclonal Antibody, 50ul Cell Proliferation Deficiency of the muscle-specific enzymeThe membrane associated protein encoded by ABCA8 is a member of the superfamily of ATP binding cassette (ABC) transporters. ABC proteins transport various molecules across extra and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in