A17454
NDUFB9 Rabbit polyclonal antibody
Size
£152.00
- SKU:
- A17454
- Additional Names:
- B22|CI-B22|LYRM3|MC1DN24|NDUFB9|UQOR22
- Application:
- ELISA, WB, IHC-P
- Molecular Weight:
- 22kDa
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C 50% glycerol. Avoid freeze/thaw cycles.
- Supplier:
- Abclonal
- Host:
- Rabbit
- Reactivities:
- Human, Mouse, Rat
- Immunogen:
- Recombinant protein (or fragment).This information is considered to be commercially sensitive.
- Formulation:
- Unmodified
- Sequence:
- YIFPDSPGGTSYERYDCYKVPEWCLDDWHPSEKAMYPDYFAKREQWKKLRRESWEREVKQLQEETPPGGPLTEALPPARKEGDLPPLWWYI
- Uniprot:
- Q9Y6M9
- Synonyms:
- B22;CI-B22;complex I B22 subunit;Complex I-B22;LYR motif-containing protein 3;LYRM3;MC1DN24;NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa;NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9;NADH-ubiquinone oxidoreductase B22 subunit;UQOR22
- Extra Details:
- 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.
- Shipping Conditions:
- Blue Ice