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NDUFB9 Antibody

  • 中文名稱:
    NDUFB9兔多克隆抗體
  • 貨號:
    CSB-PA015657GA01HU
  • 規(guī)格:
    ¥3,900
  • 其他:

產(chǎn)品詳情

  • Uniprot No.:
  • 基因名:
  • 別名:
    B22 antibody; CI B22 antibody; CI-B22 antibody; complex I B22 subunit antibody; Complex I-B22 antibody; DKFZp566O173 antibody; FLJ22885 antibody; I B22 antibody; LYR motif containing protein 3 antibody; LYR motif-containing protein 3 antibody; LYRM3 antibody; NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa antibody; NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9 antibody; NADH ubiquinone oxidoreductase B22 subunit antibody; NADH-ubiquinone oxidoreductase B22 subunit antibody; NDUB9_HUMAN antibody; Ndufb9 antibody; UQOR22 antibody
  • 宿主:
    Rabbit
  • 反應(yīng)種屬:
    Human,Mouse,Rat
  • 免疫原:
    Human NDUFB9
  • 免疫原種屬:
    Homo sapiens (Human)
  • 抗體亞型:
    IgG
  • 純化方式:
    Antigen Affinity purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
  • 產(chǎn)品提供形式:
    Liquid
  • 應(yīng)用范圍:
    ELISA,WB
  • Protocols:
  • 儲存條件:
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 貨期:
    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.
  • 用途:
    For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產(chǎn)品評價

靶點(diǎn)詳情

  • 功能:
    Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed to be not involved in catalysis. 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.
  • 基因功能參考文獻(xiàn):
    1. Down-Regulation of NDUFB9 Promotes Breast Cancer Cell Proliferation, Metastasis by Mediating Mitochondrial Metabolism. PMID: 26641458
    2. Mutant NDUFB9 is a new cause of complex I deficiency. PMID: 22200994
  • 亞細(xì)胞定位:
    Mitochondrion inner membrane; Peripheral membrane protein; Matrix side.
  • 蛋白家族:
    Complex I LYR family
  • 數(shù)據(jù)庫鏈接:

    HGNC: 7704

    OMIM: 601445

    KEGG: hsa:4715

    STRING: 9606.ENSP00000276689

    UniGene: Hs.15977