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NDUFA12 Polyclonal Antibody

规格: / 20μL / 60μL / 120μL / 200μL
价格: / ¥420 / ¥1010 / ¥1640 / ¥2365

货号:E-AB-18397

宿主: Rabbit

反应性: H,M

应用: WB,IHC

  • 详情
  • 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 Full length fusion protein
    Application WB(Detection kit: E-IR-R304),IHC(Detection kit: E-IR-R213)
    Recommended dilution WB,,1:500-1:2000;IHC,,1:25-1:100;
    Concentration 0.7mg/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 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.
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