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VWA3B Antibody

  • 中文名稱：
    VWA3B兔多克隆抗體
  • 貨號(hào)：
    CSB-PA681377LA01HU
  • 規(guī)格：
    ￥440
  • 圖片：
    • Immunohistochemistry of paraffin-embedded human skin tissue using CSB-PA681377LA01HU at dilution of 1:100
  • 其他：

產(chǎn)品詳情

  • 產(chǎn)品名稱：
    Rabbit anti-Homo sapiens (Human) VWA3B Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    VWA3B
  • 別名：
    VWA3B antibody; von Willebrand factor A domain-containing protein 3B antibody; VWA domain-containing protein 3B antibody
  • 宿主：
    Rabbit
  • 反應(yīng)種屬：
    Human
  • 免疫原：
    Recombinant Human von Willebrand factor A domain-containing protein 3B protein (1-160AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標(biāo)記方式：
    Non-conjugated

    本頁(yè)面中的產(chǎn)品，VWA3B Antibody (CSB-PA681377LA01HU)，的標(biāo)記方式是Non-conjugated。對(duì)于VWA3B Antibody，我們還提供其他標(biāo)記。見(jiàn)下表：

    可提供標(biāo)記
    標(biāo)記方式 貨號(hào) 產(chǎn)品名稱 應(yīng)用
    HRP CSB-PA681377LB01HU VWA3B Antibody, HRP conjugated ELISA
    FITC CSB-PA681377LC01HU VWA3B Antibody, FITC conjugated
    Biotin CSB-PA681377LD01HU VWA3B Antibody, Biotin conjugated ELISA
  • 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
  • 應(yīng)用范圍：
    ELISA, IHC
  • 推薦稀釋比：
    Application Recommended Dilution
    IHC 1:20-1:200
  • Protocols：
  • 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

  • 基因功能參考文獻(xiàn)：
    1. Mutated VWA3B was found to be likely associated with cerebellar degeneration with intellectual disability. Although a rare cause of cerebellar degeneration, these findings indicate a critical role for VWA3B in the apoptosis pathway in neuronal tissues. PMID: 26157035
  • 相關(guān)疾?。?/div>
    Spinocerebellar ataxia, autosomal recessive, 22 (SCAR22)
  • 亞細(xì)胞定位：
    Cytoplasm.
  • 數(shù)據(jù)庫(kù)鏈接：

    HGNC: 28385

    OMIM: 614884

    KEGG: hsa:200403

    STRING: 9606.ENSP00000417955

    UniGene: Hs.269977