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CWF19L1 Antibody

  • 货号：
    CSB-PA727965LA01HU
  • 规格：
    ￥440
  • 促销：
    小规格抗体限时一口价
  • 图片：
    • 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：

产品详情

  • 产品名称：
    Rabbit anti-Homo sapiens (Human) CWF19L1 Polyclonal antibody
  • Uniprot No.：
    Q69YN2
  • 基因名：
    CWF19L1
  • 别名：
    CWF19L1CWF19-like protein 1 antibody; C19L1 antibody
  • 宿主：
    Rabbit
  • 反应种属：
    Human
  • 免疫原：
    Recombinant Human CWF19-like protein 1 protein (101-330AA)
  • 免疫原种属：
    Homo sapiens (Human)
  • 标记方式：
    Non-conjugated

    本页面中的产品，CWF19L1 Antibody (CSB-PA727965LA01HU)，的标记方式是Non-conjugated。对于CWF19L1 Antibody，我们还提供其他标记。见下表：

    可提供标记
    标记方式 货号 产品名称 应用
    HRP CSB-PA727965LB01HU CWF19L1 Antibody, HRP conjugated ELISA
    FITC CSB-PA727965LC01HU CWF19L1 Antibody, FITC conjugated
    Biotin CSB-PA727965LD01HU CWF19L1 Antibody, Biotin conjugated ELISA
  • 克隆类型：
    Polyclonal
  • 抗体亚型：
    IgG
  • 纯化方式：
    >95%, Protein G purified
  • 浓度：
    It differs from different batches. Please contact us to confirm it.
  • 保存缓冲液：
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
  • 产品提供形式：
    Liquid
  • 应用范围：
    ELISA, WB, IHC
  • 推荐稀释比：
    Application Recommended Dilution
    WB 1:500-1:2000
    IHC 1:20-1:200
  • Protocols：
  • 储存条件：
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 货期：
    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.

产品评价

靶点详情

  • 基因功能参考文献：
    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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  • 相关疾病：
    Spinocerebellar ataxia, autosomal recessive, 17 (SCAR17)
  • 蛋白家族：
    CWF19 family
  • 组织特异性：
    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).
  • 数据库链接：

    HGNC: 25613

    OMIM: 616120

    KEGG: hsa:55280

    STRING: 9606.ENSP00000326411

    UniGene: Hs.215502