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CWF19L1 Antibody

  • 中文名稱:
    CWF19L1兔多克隆抗體
  • 貨號:
    CSB-PA727965LA01HU
  • 規格:
    ¥440
  • 圖片:
    • Western blot
      All lanes: CWF19L1 antibody at 4µg/ml + Raji whole cell lysate
      Secondary
      Goat polyclonal to rabbit IgG at 1/10000 dilution
      Predicted band size: 61, 28, 46 kDa
      Observed band size: 61 kDa
    • Immunohistochemistry of paraffin-embedded human colon tissue using CSB-PA727965LA01HU at dilution of 1:100
    • Immunohistochemistry of paraffin-embedded human pancreatic tissue using CSB-PA727965LA01HU at dilution of 1:100
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) CWF19L1 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    CWF19L1
  • 別名:
    CWF19L1CWF19-like protein 1 antibody; C19L1 antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human CWF19-like protein 1 protein (101-330AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    Non-conjugated

    本頁面中的產品,CWF19L1 Antibody (CSB-PA727965LA01HU),的標記方式是Non-conjugated。對于CWF19L1 Antibody,我們還提供其他標記。見下表:

    可提供標記
    標記方式 貨號 產品名稱 應用
    HRP CSB-PA727965LB01HU CWF19L1 Antibody, HRP conjugated ELISA
    FITC CSB-PA727965LC01HU CWF19L1 Antibody, FITC conjugated
    Biotin CSB-PA727965LD01HU CWF19L1 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
  • 產品提供形式:
    Liquid
  • 應用范圍:
    ELISA, WB, IHC
  • 推薦稀釋比:
    Application Recommended Dilution
    WB 1:500-1:2000
    IHC 1:20-1:200
  • 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.

產品評價

靶點詳情

  • 基因功能參考文獻:
    1. Our report corroborates that loss-of-function mutations in CWF19Ll lead to early onset cerebellar ataxia and (progressive) cerebellar atrophy. PMID: 27016154
    2. Two pathogenic variants in CWF19L1 were identified in a patient with autosomal recessive cerebellar ataxia. c.37G>C variant was inherited from the father and the c.946A>T variant from the mother. PMID: 26197978
    3. Results of protein-protein interaction between human Dbr1 and factors found in the Intron Large complex identify Xab2 and a novel protein CWF19L1 as specific interactors of DBR1. PMID: 25671812
    4. CWF19L1 mutations may be a novel cause of recessive ataxia with developmental delay PMID: 25361784
    5. Our findings suggest ERLIN1-CHUK-CWF19L1 variants are associated with early stage of fatty liver accumulation to hepatic inflammation. PMID: 23477746

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  • 相關疾?。?/div>
    Spinocerebellar ataxia, autosomal recessive, 17 (SCAR17)
  • 蛋白家族:
    CWF19 family
  • 組織特異性:
    Expressed in many brain regions, including cerebellum, thalamus and occipital, parietal and temporal lobes (at protein level). Also expressed in the spinal cord (at protein level).
  • 數據庫鏈接:

    HGNC: 25613

    OMIM: 616120

    KEGG: hsa:55280

    STRING: 9606.ENSP00000326411

    UniGene: Hs.215502



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