Tuberin(Phospho Tyr1571) Polyclonal Antibody, 50ul Serum & Sample Tubes Appears to link the dystrophin/utrophin

Appears to link the dystrophin/utrophin network with microtubule filaments via the syntrophins

Mutations in this gene result in cataract congenital nuclear autosomal recessive type 2

and endothelial cells

The encoded protein is a receptor for angiotensin-(1-7) and preferentially couples to the Gq protein

Diseases associated with FARP2 include verheij syndrome and aarskog-scott syndrome

Tuberin(Phospho Tyr1571) Polyclonal Antibody, 50ul Serum & Sample Tubes Appears to link the dystrophin/utrophinMutations in this gene lead to tuberous sclerosis complex. Its gene product is believed to be a tumor suppressor and is able to stimulate specific GTPases. The protein associates with hamartin in a cytosolic complex, possibly acting as a chaperone for hamartin. Alternative splicing results in multiple transcript variants encoding different isoforms.