Met(Phospho Tyr1003) Polyclonal Antibody, 20ul DNA/RNA Isolation & Purification Mutations in SPTAN1 are the

Mutations in SPTAN1 are the cause of early infantile epileptic encephalopathy-5

AQP1 encodes a small integral membrane protein with six bilayer spanning domains that functions as a water channel protein

and in addition

phosphoinositide degeneration

pancreas and thyroid and

Met(Phospho Tyr1003) Polyclonal Antibody, 20ul DNA/RNA Isolation & Purification Mutations in SPTAN1 are theThis gene encodes a member of the receptor tyrosine kinase family of proteins and the product of the proto oncogene MET. The encoded preproprotein is proteolytically processed to generate alpha and beta subunits that are linked via disulfide bonds to form the mature receptor. Further processing of the beta subunit results in the formation of the M10 peptide, which has been shown to reduce lung fibrosis. Binding of its ligand, hepatocyte growth factor,