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

Mutations in this gene cause cortical dysplasia

May play a role in subcellular trafficking between the endoplasmic reticulum and Golgi apparatus through interactions with the Rho-type GTPases

found on many cell types

The protein encoded by this gene may function as a mediator of the biological consequences of the methylation signal

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