NDUFS3 Polyclonal Antibody, 50ul Glassware Sets making them perfect for ambient

making them perfect for ambient shipping

Mutations in this gene may underlie hereditary disorders of balance and hearing

Multiple pseudogenes on chromosome 9

This gene encodes a member of the L-amino acid transporter-3 or SLC43 family of transporters

indicating that the gene is essential for normal postnatal skeletal growth and cartilage homeostasis

NDUFS3 Polyclonal Antibody, 50ul Glassware Sets making them perfect for ambientNDUFS3 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.