AT10A Rabbit Polyclonal Antibody, 100ul Mammalian Expression Defects in EIF2B4 are a

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

This receptor mediates most if not all of the biological effects of this cytokine

It is a catalytic subunit of the protein kinase complex that is important for cell cycle G1 phase progression

and two beta subunits

SFRP2 encodes a member of the SFRP family that contains a cysteine-rich domain homologous to the putative Wnt-binding site of Frizzled proteins

AT10A Rabbit Polyclonal Antibody, 100ul Mammalian Expression Defects in EIF2B4 are aThe 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'.