GTX67583-PRO
Human NDUFB9 protein, His tag
Cannot supply to this region.
- SKU:
- GTX67583-PRO
- Additional Names:
- NADH:ubiquinone oxidoreductase subunit B9 , B22 , CI-B22 , LYRM3 , MC1DN24 , UQOR22
- Concentration:
- 0.25 mg/ml
- Physical State:
- Liquid
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Buffer:
- 20mM Tris-HCl, 0.4M Urea, 10% Glycerol, no preservatives.
- Immunogen:
- NADH:ubiquinone oxidoreductase subunit B9
- Species:
- Human
- 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. [provided by RefSeq, Jul 2015]
- Shipping Conditions:
- Dry Ice