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  4. TTI2 Antibody, FITC conjugated

TTI2 Antibody, FITC conjugated

  • 中文名稱：
    TTI2兔多克隆抗體, FITC偶聯(lián)
  • 貨號：
    CSB-PA764687LC01HU
  • 規(guī)格：
    ￥880
  • 其他：

產(chǎn)品詳情

  • 產(chǎn)品名稱：
    Rabbit anti-Homo sapiens (Human) TTI2 Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    TTI2
  • 別名：
    C8orf41 antibody; CH041_HUMAN antibody; TELO2 interacting protein 2provided antibody; TTI2 antibody; Uncharacterized protein C8orf41 antibody
  • 宿主：
    Rabbit
  • 反應(yīng)種屬：
    Human
  • 免疫原：
    Recombinant Human TELO2-interacting protein 2 protein (159-264AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標記方式：
    FITC
  • 克隆類型：
    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

靶點詳情

  • 功能：
    Regulator of the DNA damage response (DDR). Part of the TTT complex that is required to stabilize protein levels of the phosphatidylinositol 3-kinase-related protein kinase (PIKK) family proteins. The TTT complex is involved in the cellular resistance to DNA damage stresses, like ionizing radiation (IR), ultraviolet (UV) and mitomycin C (MMC). Together with the TTT complex and HSP90 may participate in the proper folding of newly synthesized PIKKs.
  • 基因功能參考文獻：
    1. The findings emphasises the role of the TTI2 gene in the etiology of intellectual disability. PMID: 23956177
    2. TTI1 and TTI2 protect cells from spontaneous DNA damage, and are required for the establishment of the intra-S and G2/M checkpoint. PMID: 20810650
  • 相關(guān)疾病：
    Mental retardation, autosomal recessive 39 (MRT39)
  • 蛋白家族：
    TTI2 family
  • 數(shù)據(jù)庫鏈接：

    HGNC: 26262

    OMIM: 614426

    KEGG: hsa:80185

    STRING: 9606.ENSP00000353971

    UniGene: Hs.742048



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