AT10A Rabbit Polyclonal Antibody, 100ul Mammalian Expression and both the translated and

and both the translated and the untranslated regions show a high degree of sequence similarity to the rat gene

also known as factor B

Defects in EIF2B4 are a cause of leukoencephalopathy with vanishing white matter (VWM) and ovarioleukodystrophy

ubiquitin aldehyde binding 2 contains an OTU domain and binds Ubal (ubiquitin aldehyde)

and two beta subunits

AT10A Rabbit Polyclonal Antibody, 100ul Mammalian Expression and both the translated andThe 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'.