SMG9 Polyclonal Antibody, 20ul CellSafe™ It is required for maximal

It is required for maximal stimulated calcium release after stimulation of purinergic or muscarinic but not beta-adrenergic receptors

13) involving this gene is associated with X-linked mental retardation

This gene is a susceptibility gene for Moyamoya disease| a vascular disorder of intracranial arteries

The protein encoded by this gene may function as a mediator of the biological consequences of the methylation signal

The protein is a calcium(2+)-independent cell-cell adhesion molecule that belongs to the immunoglobulin superfamily and has 3 extracellular immunoglobulin-like loops

SMG9 Polyclonal Antibody, 20ul CellSafe™ It is required for maximalThis gene encodes a regulatory subunit of the SMG1 complex, which plays a critical role in nonsense mediated mRNA decay (NMD). Binding of the encoded protein to the SMG1 complex kinase scaffold protein results in the inhibition of its kinase activity. Mutations in this gene cause a multiple congenital anomaly syndrome in human patients, characterized by brain malformation, congenital heart disease and other features.