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  4. FIGN Antibody, HRP conjugated

FIGN Antibody, HRP conjugated

说明书
  • 中文名称：
    FIGN兔多克隆抗体, HRP偶联
  • 货号：
    CSB-PA008676LB01HU
  • 规格：
    ￥880
  • 其他：

产品详情

  • 产品名称：
    Rabbit anti-Homo sapiens (Human) FIGN Polyclonal antibody
  • Uniprot No.：
    Q5HY92
  • 基因名：
    FIGN
  • 别名：
    FIGNFidgetin antibody
  • 宿主：
    Rabbit
  • 反应种属：
    Human
  • 免疫原：
    Recombinant Human Fidgetin protein (132-371AA)
  • 免疫原种属：
    Homo sapiens (Human)
  • 标记方式：
    HRP
  • 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
  • Protocols：
    ELISA Protocol
  • 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.
  • 用途：
    For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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FIGN antibodies

FIGN Proteins

靶点详情

  • 功能：
    ATP-dependent microtubule severing protein. Severs microtubules along their length and depolymerizes their ends, primarily the minus-end, that may lead to the suppression of microtubule growth from and attachment to centrosomes. Microtubule severing may promote rapid reorganization of cellular microtubule arrays and the release of microtubules from the centrosome following nucleation. Microtubule release from the mitotic spindle poles may allow depolymerization of the microtubule end proximal to the spindle pole, leading to poleward microtubule flux and poleward motion of chromosome.
  • 基因功能参考文献：
    1. FIGN might play an important role in decreased congenital heart defect risk by upregulating plasma folate concentration during embryo heart development PMID: 28534241
    2. FIGN +94762G>C polymorphism reduced the risk of congenital heart defects by activating the transcription of an alternative FIGN isoform, inhibiting proteasome activity and allowing the accumulation of RFC1 and DHFR, promoting folate transmembrane transport and utilization. PMID: 28302752
    3. The loss of Fidgetin induces a microtubule-dependent enlargement of mitotic centrosomes and an increase in the number and length of astral microtubules. PMID: 22672901
  • 亚细胞定位：
    Nucleus matrix. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome. Note=Localizes to centrosomes throughout mitosis and to the spindle midzone during telophase.
  • 蛋白家族：
    AAA ATPase family
  • 数据库链接：

    HGNC: 13285

    OMIM: 605295

    KEGG: hsa:55137

    STRING: 9606.ENSP00000333836

    UniGene: Hs.593650

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