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AASS Antibody, FITC conjugated

  • 中文名稱(chēng)：
    AASS兔多克隆抗體, FITC偶聯(lián)
  • 貨號(hào)：
    CSB-PA883373LC01HU
  • 規(guī)格：
    ￥880
  • 其他：

產(chǎn)品詳情

  • 產(chǎn)品名稱(chēng)：
    Rabbit anti-Homo sapiens (Human) AASS Polyclonal antibody
  • Uniprot No.：
  • 基因名：
  • 別名：
    AASSAlpha-aminoadipic semialdehyde synthase antibody; mitochondrial antibody; LKR/SDH) [Includes: Lysine ketoglutarate reductase antibody; LKR antibody; LOR antibody; EC 1.5.1.8); Saccharopine dehydrogenase antibody; SDH antibody; EC 1.5.1.9)] antibody
  • 宿主：
    Rabbit
  • 反應(yīng)種屬：
    Human
  • 免疫原：
    Recombinant Human Alpha-aminoadipic semialdehyde synthase, mitochondrial protein (224-364AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標(biāo)記方式：
    FITC
  • 克隆類(lèi)型：
    Polyclonal
  • 抗體亞型：
    IgG
  • 純化方式：
    >95%, Protein G purified
  • 濃度：
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液：
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
  • 產(chǎn)品提供形式：
    Liquid
  • 儲(chǔ)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(píng)價(jià)

靶點(diǎn)詳情

  • 功能：
    Bifunctional enzyme that catalyzes the first two steps in lysine degradation. The N-terminal and the C-terminal contain lysine-ketoglutarate reductase and saccharopine dehydrogenase activity, respectively.
  • 基因功能參考文獻(xiàn)：
    1. GR and KLF15 physically interact via low affinity GR binding sites within glucocorticoid response elements (GREs) for PRODH and AASS that contribute to combinatorial regulation with KLF15. PMID: 26088140
    2. Mitochondrial NADPH is crucial for AASS function PMID: 24847004
    3. Hyperlysinemia is caused by mutations in AASS PMID: 23570448
    4. Isolation and characterization of the mouse ortholog. PMID: 10567240
  • 相關(guān)疾?。?/div>
    Hyperlysinemia, 1 (HYPLYS1); 2,4-dienoyl-CoA reductase deficiency (DECRD)
  • 亞細(xì)胞定位：
    Mitochondrion.
  • 蛋白家族：
    AlaDH/PNT family; Saccharopine dehydrogenase family
  • 組織特異性：
    Expressed in all 16 tissues examined with highest expression in the liver.
  • 數(shù)據(jù)庫(kù)鏈接：

    HGNC: 17366

    OMIM: 238700

    KEGG: hsa:10157

    STRING: 9606.ENSP00000377040

    UniGene: Hs.156738