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FYCO1 Antibody, Biotin conjugated

  • 中文名称:
    FYCO1兔多克隆抗体, Biotin偶联
  • 货号:
    CSB-PA866262LD01HU
  • 规格:
    ¥880
  • 其他:

产品详情

  • 产品名称:
    Rabbit anti-Homo sapiens (Human) FYCO1 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
  • 别名:
    CATC2 antibody; CTRCT18 antibody; DKFZp779K1152 antibody; FLJ13335 antibody; FYCO1 antibody; FYCO1_HUMAN antibody; FYVE and coiled coil domain containing 1 antibody; FYVE and coiled coil domain containing protein 1 antibody; FYVE and coiled-coil domain-containing protein 1 antibody; MGC126517 antibody; MGC126519 antibody; RUFY3 antibody; RUN and FYVE domain containing 3 antibody; ZFYVE7 antibody; Zinc finger FYVE domain containing protein 7 antibody; Zinc finger FYVE domain-containing protein 7 antibody
  • 宿主:
    Rabbit
  • 反应种属:
    Human
  • 免疫原:
    Recombinant Human FYVE and coiled-coil domain-containing protein 1 protein (2-255AA)
  • 免疫原种属:
    Homo sapiens (Human)
  • 标记方式:
    Biotin
  • 克隆类型:
    Polyclonal
  • 抗体亚型:
    IgG
  • 纯化方式:
    Antigen Affinity 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:
  • 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.

产品评价

靶点详情

  • 功能:
    May mediate microtubule plus end-directed vesicle transport.
  • 基因功能参考文献:
    1. FYCO1 regulates accumulation of post-mitotic midbodies by mediating LC3-dependent midbody degradation PMID: 29196475
    2. FYCO1 and MAP1LC3A interact through a novel binding mode that involves Atg8-family proteins PMID: 27246247
    3. Rare missense variants in FYCO1 are overrepresented in sporadic inclusion body myositis patients. PMID: 28009083
    4. FYCO1 requires a functional LC3A/B-preferring LC3-interacting Region (LIR) motif to facilitate efficient maturation of autophagosomes under basal conditions, whereas starvation-induced autophagy was unaffected PMID: 26468287
    5. FYCO1 is involved in lens development and transparency in humans, and mutations in this gene are one of the most common causes of autosomal-recessive congenital cataracts in the Pakistani population. PMID: 21636066
    6. We have characterized the LC3-, Rab7-, and phosphatidylinositol-3-phosphate-binding domains in FYCO1 and mapped part of the CC region essential for MT plus end-directed transport. PMID: 20100911
    7. Maps to a region of chromosome 3p21.3 which is frequently deleted in tumors. PMID: 11896456

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  • 相关疾病:
    Cataract 18 (CTRCT18)
  • 亚细胞定位:
    Cytoplasmic vesicle, autophagosome. Endosome. Lysosome. Note=Localizes to the external but not to the internal membrane of autophagosomes, and upon autophagosome/late endosome/lysosome fusion, it stays on the external surface of autolysosomes.
  • 组织特异性:
    Expressed in heart and skeletal muscle.
  • 数据库链接:

    HGNC: 14673

    OMIM: 607182

    KEGG: hsa:79443

    STRING: 9606.ENSP00000296137

    UniGene: Hs.200227