AT10A Rabbit Polyclonal Antibody, 50ul Cellular Cultivation & Health Management Capacity：2mL × 40 Diameter×depth：11×34

Capacity：2mL × 40 Diameter×depth：11×34

Mutations in this gene may be involved in the cause of familial idiopathic pulmonary fibrosis

and type II deficiency

Mutations in this gene have been associated with Andersen syndrome

members of which mediate signal transduction by binding to phosphoserine-containing proteins

AT10A Rabbit Polyclonal Antibody, 50ul Cellular Cultivation & Health Management Capacity：2mL × 40 Diameter×depth：11×34The protein encoded by this gene belongs to the family of P type cation transport ATPases, and to the subfamily of aminophospholipid transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to another. This gene is maternally expressed. It maps within the most common interval of deletion responsible for Angelman syndrome, also known as 'happy puppet syndrome'.