Human NDUFB9 protein, His tag

GeneTex

Human NDUFB9 protein, His tag

9

Research Use Only

0.25 mg/ml

Unconjugated

NDUFB9

NADH:ubiquinone oxidoreductase subunit B9

B22, CI-B22, LYRM3, MC1DN24, UQOR22, NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9, LYR motif-containing protein 3, NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa, NADH-ubiquinone oxidoreductase B22 subunit, complex I B22 subunit

NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9

The protein encoded by this gene 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 phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]

-20°C or -80°C,2°C to 8°C

41116100

Human