A17454
NDUFB9 Rabbit polyclonal antibody
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£152.00
- SKU:
- A17454
- Zusätzliche Namen:
- B22|CI-B22|LYRM3|MC1DN24|NDUFB9|UQOR22
- Anwendung:
- ELISA, WB, IHC-P
- Molekulargewicht:
- 22kDa
- Spezies-Reaktivität:
- Human
- Aufreinigung:
- Affinity Purified
- Lagerbedingungen:
- -20[o]C 50% glycerol. Avoid freeze/thaw cycles.
- Hersteller:
- Abclonal
- Host:
- Rabbit
- Reaktivitäten:
- Human, Mouse, Rat
- Immunogen:
- Recombinant protein (or fragment).This information is considered to be commercially sensitive.
- Formulierung:
- Unmodified
- Sequenz:
- YIFPDSPGGTSYERYDCYKVPEWCLDDWHPSEKAMYPDYFAKREQWKKLRRESWEREVKQLQEETPPGGPLTEALPPARKEGDLPPLWWYI
- Uniprot:
- Q9Y6M9
- Synonyme:
- 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
- Weitere 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.
- Versandbedingungen:
- Blue Ice