This gene encodes a mitochondrial complex I assemblynprotein that interacts with complex I subunits. Mutations in thisngene cause mitochondrial complex I deficiency, a fatal neonatalndisorder of the oxidative phosphorylation system. Alternativelynspliced transcript variants encoding different isoforms have beennidentified.
应用类型
WB,IHC
免疫原
This NDUF3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 12-40 amino acids from the N-terminal region of human NDUF3.
