AT10A Rabbit Polyclonal Antibody, 100ul Mammalian Expression and as a heterodimer with

and as a heterodimer with a similar brain isozyme in heart

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

and two beta subunits

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

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

AT10A Rabbit Polyclonal Antibody, 100ul Mammalian Expression and as a heterodimer withThe 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'.