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Antibody detects endogenous levels of total ATPAF2.
This gene 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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: ATP synthase mitochondrial F1 complex assembly factor 2; ATP12 homolog
Gene Aliases: ATP12; ATP12p; ATPAF2; LP3663; MC5DN1
UniProt ID: (Human) Q8N5M1, (Mouse) Q91YY4
Entrez Gene ID: (Human) 91647, (Mouse) 246782
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