MAO-A Polyclonal Antibody, 100ul[BT-AP05200] Rotator Solute carrier family 22 member

Solute carrier family 22 member 3 contains twelve putative transmembrane domains and is a plasma integral membrane protein

Most WFDC genes are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric

which possesses potent spasmogenic and chemotactic activity

Read-through transcription exists between GIMAP5 and the neighboring upstream GIMAP1 (GTPase

MAO-A Polyclonal Antibody, 100ul[BT-AP05200] Rotator Solute carrier family 22 memberMAOA is one of two neighboring gene family members that encode Amine oxidase [flavin containing] A which catalyze the oxidative deamination of amines, such as dopamine, norepinephrine, and serotonin. Mutation of this gene results in Brunner syndrome. This gene has also been associated with a variety of other psychiatric disorders, including antisocial behavior. Alternatively spliced transcript variants encoding multiple isoforms have been observed.