NDUFS3 polyclonal, anti-human
€426.00
In stock
SKU
AC-AF1713a
Background:
This gene encodes one of the iron-sulfur protein (IP) components of mitochondrial NADH:ubiquinone oxidoreductase (complex I). Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency.
Other Names:
NADH dehydrogenase [ubiquinone] iron-sulfur protein 3, mitochondrial, 1.6.5.3, 1.6.99.3, Complex I-30kD, CI-30kD, NADH-ubiquinone oxidoreductase 30 kDa subunit, NDUFS3
Antigen Types:
Synthetic Peptide
Gene Name:
NDUFS3
Gene ID:
4722
Primary Accession: O75489
Other Accession: NP_004542;4722;
This gene encodes one of the iron-sulfur protein (IP) components of mitochondrial NADH:ubiquinone oxidoreductase (complex I). Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency.
Other Names:
NADH dehydrogenase [ubiquinone] iron-sulfur protein 3, mitochondrial, 1.6.5.3, 1.6.99.3, Complex I-30kD, CI-30kD, NADH-ubiquinone oxidoreductase 30 kDa subunit, NDUFS3
Antigen Types:
Synthetic Peptide
Gene Name:
NDUFS3
Gene ID:
4722
Primary Accession: O75489
Other Accession: NP_004542;4722;
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