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NDUFB3 encodes an accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which is the first enzyme in the electron transport chain of mitochondria. Additionally we are shipping NDUFB3 Antibodies (25) and and many more products for this protein.
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Recessive mutations in NDUFB3 cause complex I deficiency
This gene encodes an accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which is the first enzyme in the electron transport chain of mitochondria. This protein localizes to the inner membrane of the mitochondrion as a single-pass membrane protein. Mutations in this gene contribute to mitochondrial complex 1 deficiency. Alternative splicing results in multiple transcript variants encoding the same protein. Humans have multiple pseudogenes of this gene.
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3 , NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 3, 12kDa , NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 3 , OXPHOS complex I B12 subunit , CI-B12 , NADH-ubiquinone oxidoreductase B12 subunit , complex I-B12 , mitochondrial complex I subunit NDUFB3