RGS1 Polyclonal Antibody, 50ul[BT-AP07798] Plasmid Preparation Mutations in this gene are

Mutations in this gene are associated with type II autosomal recessive Alport syndrome (hereditary glomerulonephropathy) and with familial benign hematuria (thin basement membrane disease)

This gene encodes a protein that was identified as being similar to the Drosophila scribble protein

RNF149 (Ring Finger Protein 149) is a Protein Coding gene

as well as by an interleukin 4 receptor-associated kinase in response to IL4 treatment

transcription termination factor 1

RGS1 Polyclonal Antibody, 50ul[BT-AP07798] Plasmid Preparation Mutations in this gene areRGS1 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