Synphilin-1 Polyclonal Antibody, 50ul Rotator GTPase-activating proteins

GTPase-activating proteins

Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD)

It is essential for disk morphogenesis| and may also function as an adhesion molecule involved in the stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim

As an essential component of MAP kinase signal transduction pathway

Synphilin-1 Polyclonal Antibody, 50ul Rotator GTPase-activating proteinsSNCAIP encodes Synphilin 1 containing several protein protein interaction domains, including ankyrin like repeats, a coiled coil domain, and an ATP GTP binding motif. The synphilin 1 interacts with alpha synuclein in neuronal tissue and may play a role in the formation of cytoplasmic inclusions and neurodegeneration. A mutation in this gene has been associated with Parkinson's disease. Alternative splicing results in multiple transcript variants.