ATPAF2 Polyclonal Antibody, 20ul Protein Post-translational Modification and can be distinguished by

and can be distinguished by their electrophoretic mobility

Mutations in AKT1 have been associated with the Proteus syndrome

AIFM2 encodes a flavoprotein oxidoreductase (apoptosis inducing factor

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ATPAF2 Polyclonal Antibody, 20ul Protein Post-translational Modification and can be distinguished byATPAF2 encodes an assembly factor for the F (1) component of the mitochondrial ATP synthase. This protein binds specifically to the F1 alpha subunit and is thought to prevent this subunit from forming nonproductive homooligomers during enzyme assembly. This gene is located within the Smith Magenis syndrome region on chromosome 17. An alternatively spliced transcript variant has been described, but its biological validity has not been determined.