NDUFA2 Polyclonal Antibody
规格: | / 20μL / 60μL / 120μL / 200μL |
价格: | / ¥420 / ¥1010 / ¥1640 / ¥2365 |
货号:E-AB-18269
宿主: Rabbit
反应性: H
应用: IHC
Overview
Synonyms | B8,CI B8,CI-B8,Complex I B8,Complex I-B8,NADH dehydrogenase (ubiquinone) 1 alpha subcomplex 2 8kDa,NADH dehydrogenase (ubiquinone) 1 alpha subcomplex 2,NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2,NADH ubiquinone oxidoreductase B8 subunit,NADH-ubiquinone oxidoreductase B8 subunit,NDUA2,NDUFA 2,Ndufa2,NDUFA2抗体 |
Swissprot | O43678 |
Source | Rabbit |
Reactivity | Human |
Immunogen | Fusion protein of human NDUFA2 |
Application | IHC(Detection kit: E-IR-R213) |
Recommended dilution | IHC,,1:50-1:100 |
Concentration | 0.96mg/mL |
Clonality | Polyclonal |
Properties
Cellular localization | Mitochondrion inner membrane. |
Isotype | IgG |
Purification | Affinity purification |
Conjugation | Unconjugated |
Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
Storage buffer | PBS with 0.05% NaN3 and 40% Glycerol,pH7.4 |
Background | The encoded protein is a subunit of the hydrophobic protein fraction of the NADH:ubiquinone oxidoreductase (complex 1), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane, and may be involved in regulating complex I activity or its assembly via assistance in redox processes. Mutations in this gene are associated with Leigh syndrome, an early-onset progressive neurodegenerative disorder. |