ATPAF2 Polyclonal Antibody, 20ul Protein Post-translational Modification Unlock the full potential of

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and can be distinguished by their electrophoretic mobility

Mutations in AKT1 have been associated with the Proteus syndrome

ATPAF2 Polyclonal Antibody, 20ul Protein Post-translational Modification Unlock the full potential ofATPAF2 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.