NDUFA12 Polyclonal Antibody
| 规格： | / 20μL / 60μL / 120μL / 200μL |
| 价格： | / ￥420 / ￥1010 / ￥1640 / ￥2365 |
货号：E-AB-15597
宿主: Rabbit
反应性: H,M
应用: IHC
Overview
| Synonyms | 13 kDa differentiation associated protein,13 kDa differentiation-associated protein,2410011G03Rik,AW112974,B17.2,CI-B17.2,CIB17.2,Complex I B17.2,Complex I B17.2 subunit,Complex I-B17.2,DAP13,MGC107642,MGC7999,NADH dehydrogenase (ubiquinone) 1 alpha subcomplex 12,NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12,NADH ubiquinone oxidoreductase subunit B17.2,NADH-ubiquinone oxidoreductase subunit B17.2,NDUAC,NDUFA12,RGD1311462,NDUFA12抗体 |
| Swissprot | Q9UI09 |
| Source | Rabbit |
| Reactivity | Human,Mouse |
| Immunogen | Synthetic peptide of human NDUFA12 |
| Application | IHC(Detection kit: E-IR-R213) |
| Recommended dilution | IHC,,1:50-1:200 |
| Concentration | 0.4 mg/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% sodium azide, 50% glycerol, PH7.3 |
| Background | This gene encodes a protein which is part of mitochondrial complex 1, part of the oxidative phosphorylation system in mitochondria. Complex 1 transfers electrons to ubiquinone from NADH which establishes a proton gradient for the generation of ATP. Mutations in this gene are associated with Leigh syndrome due to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13. Alternative splicing results in multiple transcript variants. |
