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NADH transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. Additionally we are shipping NDUFAF4 Antibodies (28) and many more products for this protein.
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A homozygous missense NDUFAF4 variant was identified in a complex I-deficient patient with Leigh syndrome.
observations suggest that HRPAP20 may be an important regulator of breast tumor cell invasion by a CaM-mediated mechanism that leads to increased MMP-9 (show MMP9 Proteins) secretion
HRPAP20 and TIMELESS as promising markers of tamoxifen resistance in women with ER alpha (show ESR1 Proteins)-positive breast tumors.
Homozygosity mapping of 5 patients from a consanguineous family with infantile mitochondrial encephalomyopathy resulted in the identification of a missense mutation in a conserved residue of the C6ORF66.
Mutations in NDUFAF3 (C3ORF60 (show NDUFAF3 Proteins)), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial disease.
NADH transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. This gene encodes a complex I assembly factor. Mutations in this gene are a cause of mitochondrial complex I deficiency.
NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 4
, NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 4
, hormone-regulated proliferation-associated protein of 20 kDa homolog
, Protein HRPAP20
, hormone-regulated proliferation-associated protein of 20 kDa
, hormone-regulated proliferation-associated protein, 20 kDa
, hormone-regulated proliferation associated protein 20
, hormone-regulated proliferation-associated 20 kDa protein