NDUFB9 Polyclonal Antibody, 100ul Peptide Synthesis Mutations in this gene cause

Mutations in this gene cause cortical dysplasia

This gene belongs to the KCNN family of potassium channels

It has been suggested to be involved in several basic biological events such as cell death

coli adhesion to the surface of ileal epithelial cells in patients with Crohn's disease

NDUFB9 Polyclonal Antibody, 100ul Peptide Synthesis Mutations in this gene causeNADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 10 encoded by NDUFB9 is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative