RGS1 Polyclonal Antibody, 100ul[BT-AP07799] Cell Labeling & Imaging Mutations in STXBP1 have been

Mutations in STXBP1 have been associated with infantile epileptic encephalopathy-4

Diseases associated with SLC5A6 include thiamine metabolism dysfunction syndrome 2 and urinary tract obstruction

NVL encodes a member of the AAA (ATPases associated with diverse cellular activities) superfamily

as well as in cell-cell and cell-matrix adhesion signaling

RGS1 Polyclonal Antibody, 100ul[BT-AP07799] Cell Labeling & Imaging Mutations in STXBP1 have beenRGS1 encodes a member of the regulator of G protein signalling family. Regulator of G protein signaling 1 is located on the cytosolic side of the plasma membrane and contains a conserved, 120 amino acid motif called the RGS domain. The protein attenuates the signalling activity of G proteins by binding to activated, GTP bound G alpha subunits and acting as a GTPase activating protein (GAP), increasing the rate of conversion of the GTP to GDP. This