8ODP Polyclonal Antibody, 50ul Shaker&Mixing ccessory component of a P4-ATPase

ccessory component of a P4-ATPase flippase complex which catalyzes the hydrolysis of ATP coupled to the transport of aminophospholipids from the outer to the inner leaflet of various membranes and ensures the maintenance of asymmetric distribution of phospholipids

MIM 139310) and Gq (see GNAQ

whereas the released C-terminal fragment is an EMAP II-like cytokine

Mutations in this gene have been associated with Kenny-Caffey syndrome (KCS) type 2 and the more severe osteocraniostenosis (OCS| also known as Gracile Bone Dysplasia)| both characterized by short stature| hypoparathyroidism| bone development abnormalities| and hypocalcemia

Found in a complex with XPO7

8ODP Polyclonal Antibody, 50ul Shaker&Mixing ccessory component of a P4-ATPaseMisincorporation of oxidized nucleoside triphosphates into DNA RNA during replication and transcription can cause mutations that may result in carcinogenesis or neurodegeneration. The protein encoded by this gene is an enzyme that hydrolyzes oxidized purine nucleoside triphosphates such as 8 oxo dGTP 8 oxo dATP 2 hydroxy dATP and 2 hydroxy rATP to monophosphates thereby preventing misincorporation. The encoded protein is localized mainly in the