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Cell line expression
Protein structure
NDUFB9
NADH:ubiquinone oxidoreductase subunit B9B22, LYRM3, UQOR22
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]
Top validated antibodies |
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| LSBio |  LS-C172622 |
Monoclonal |
WB
IHC
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| Invitrogen Antibodies | MA5-44793 |
Monoclonal |
WB
ICC
IHC
FC
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| Proteintech Group | 15572-1-AP |
2 references | Polyclonal |
WB
EL
IHC
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| Biorbyt | orb1726628 |
Recombinant |
WB
ICC
IP
IHC
FC
|
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| Novus Biologicals | NBP1-77138 |
Polyclonal |
WB
EL
ICC
IHC
|
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