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  4. SYNC Antibody, FITC conjugated

SYNC Antibody, FITC conjugated

  • 中文名稱：
    SYNC兔多克隆抗體, FITC偶聯
  • 貨號：
    CSB-PA862034LC01HU
  • 規格：
    ￥880
  • 其他：

產品詳情

  • 產品名稱：
    Rabbit anti-Homo sapiens (Human) SYNC Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    SYNC
  • 別名：
    1110057H03Rik antibody; Intermediate filament protein syncoilin antibody; MGC124230 antibody; MGC149625 antibody; MGC149626 antibody; RP23-391E6.2 antibody; SNIP4 antibody; SYNC antibody; SYNC1 antibody; SYNCI_HUMAN antibody; Syncoilin antibody; Syncoilin intermediate filament 1 antibody; Syncoilin-1 antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Recombinant Human Syncoilin protein (332-482AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標記方式：
    FITC
  • 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
  • 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

  • 功能：
    Atypical type III intermediate filament (IF) protein that may play a supportive role in the efficient coupling of mechanical stress between the myofibril and fiber exterior. May facilitate lateral force transmission during skeletal muscle contraction. Does not form homofilaments nor heterofilaments with other IF proteins.
  • 基因功能參考文獻：
    1. Syncoilin modulates peripherin filament network formation. PMID: 20587592
    2. The differences in human syncoilin and beta-synemin mRNA ratios between Duchenne muscular dystrophy and normal muscles were not statistically significant PMID: 20199207
    3. the result of this study raise the possibility that mutations in the gene encoding for syncoilin may underlie some forms of muscle disease. PMID: 16124004
  • 亞細胞定位：
    Cytoplasm, perinuclear region.
  • 蛋白家族：
    Intermediate filament family
  • 數據庫鏈接：

    HGNC: 28897

    OMIM: 611750

    KEGG: hsa:81493

    STRING: 9606.ENSP00000386439

    UniGene: Hs.712631



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