MYPT1(Phospho-Ser507) Rabbit Polyclonal Antibody, 20ul Peripheral Blood Separation Tube Mutations in this gene cause

Mutations in this gene cause combined oxidative phosphorylation deficiency 6 (COXPD6)

The protein directly interacts with several components of the NPC

Plays a role in the formation of lamellipodia and in cell migration

Prostaglandin E receptor 3 encoded by PTGER3 is a member of the G-protein coupled receptor family

It is prposed that this protein is involved in the attachment of the inner ear acellular gels to the apical surface of the underlying nonsensory cells

MYPT1(Phospho-Ser507) Rabbit Polyclonal Antibody, 20ul Peripheral Blood Separation Tube Mutations in this gene causeMyosin phosphatase target subunit 1 which is also called the myosin binding subunit of myosin phosphatase is one of the subunits of myosin phosphatase. Myosin phosphatase regulates the interaction of actin and myosin downstream of the guanosine triphosphatase Rho. The small guanosine triphosphatase Rho is implicated in myosin light chain (MLC) phosphorylation which results in contraction of smooth muscle and interaction of actin and myosin in