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NDUFA9 Antibody

  • 货号：
    CSB-PA015634GA01HU
  • 规格：
    ￥3,900
  • 其他：

产品详情

  • Uniprot No.：
    Q16795
  • 基因名：
  • 别名：
    CI-39kD antibody; Complex I subunit NDUFA9 antibody; Complex I-39kD antibody; mitochondrial antibody; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9 antibody; NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 9 mitochondrial antibody; NADH Ubiquinone Oxidoreductase 1 alpha subcomplex 9 antibody; NADH-ubiquinone oxidoreductase 39 kDa subunit antibody; NDUA9_HUMAN antibody; NDUFA9 antibody
  • 宿主：
    Rabbit
  • 反应种属：
    Human,Mouse,Rat
  • 免疫原：
    Human NDUFA9
  • 免疫原种属：
    Homo sapiens (Human)
  • 抗体亚型：
    IgG
  • 纯化方式：
    Antigen Affinity purified
  • 浓度：
    It differs from different batches. Please contact us to confirm it.
  • 保存缓冲液：
    PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
  • 产品提供形式：
    Liquid
  • 应用范围：
    ELISA,WB,IHC
  • Protocols：
  • 储存条件：
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 货期：
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

产品评价

靶点详情

  • 功能：
    Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in catalysis. Required for proper complex I assembly. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone.
  • 基因功能参考文献：
    1. NDUFA9 protein is essential for stabilizing the junction between membrane and matrix arms of complex I. PMID: 23223238
    2. A pathogenic mutation was found in the complex I subunit encoding the NDUFA9 gene, changing a highly conserved arginine at position 321 to proline PMID: 22114105
    3. Study identifies mitochondrial transit peptide and determines mature protein cleavage site in cow ortholog. PMID: 1832859
  • 相关疾病：
    Leigh syndrome (LS)
  • 亚细胞定位：
    Mitochondrion matrix.
  • 蛋白家族：
    Complex I NDUFA9 subunit family
  • 数据库链接：

    HGNC: 7693

    OMIM: 256000

    KEGG: hsa:4704

    STRING: 9606.ENSP00000266544

    UniGene: Hs.75227