OGT(Phospho Thr454) Rabbit Polyclonal Antibody, 50ul ROS/Nitric Oxide Detection Mutations in this gene may

Mutations in this gene may be associated with susceptibility to carotid artery disease

Defects in this gene cause Hailey-Hailey disease

Ghrelin is thought to regulate multiple activities

including axon guidance

Also targets the mutant SOD1 protein involved in familial amyotrophic lateral sclerosis (FALS)

OGT(Phospho Thr454) Rabbit Polyclonal Antibody, 50ul ROS/Nitric Oxide Detection Mutations in this gene mayThis gene encodes a glycosyltransferase that catalyzes the addition of a single N acetylglucosamine in O glycosidic linkage to serine or threonine residues. Since both phosphorylation and glycosylation compete for similar serine or threonine residues the two processes may compete for sites or they may alter the substrate specificity of nearby sites by steric or electrostatic effects. The protein contains multiple tetratricopeptide repeats that are