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DOK7 抗体

DOK7 适用: 人 WB, IF 宿主: 小鼠 Monoclonal 4C6 unconjugated
产品编号 ABIN2719655
发货至: 中国
  • 抗原 See all DOK7 抗体
    DOK7 (Docking Protein 7 (DOK7))
    适用
    • 29
    • 25
    • 16
    宿主
    • 46
    • 4
    • 1
    • 1
    小鼠
    克隆类型
    • 48
    • 4
    单克隆
    标记
    • 17
    • 5
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This DOK7 antibody is un-conjugated
    应用范围
    • 41
    • 22
    • 13
    • 13
    • 7
    • 7
    • 6
    • 3
    • 3
    • 3
    Western Blotting (WB), Immunofluorescence (IF)
    产品特性
    Homo sapiens docking protein 7 (DOK7), transcript variant 1
    纯化方法
    Purified from mouse ascites fluids by affinity chromatography
    免疫原
    Full length human recombinant protein of human DOK7(NP_775931) produced in HEK293T cell.
    克隆位点
    4C6
    亚型
    IgG1
    Top Product
    Discover our top product DOK7 Primary Antibody
  • 应用备注
    WB 1:2000, IF 1:100,
    说明

    The concentration of the product may vary between diferrent lots.

    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.5-1.0 mg/mL
    缓冲液
    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.
    储存液
    Sodium azide
    注意事项
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
  • 抗原
    DOK7 (Docking Protein 7 (DOK7))
    别名
    DOK7 (DOK7 产品)
    别名
    si:dkey-180b4.3 antibody, si:ch211-164d19.2 antibody, C4orf25 antibody, CMS1B antibody, A930013K19Rik antibody, AW049091 antibody, Dok-7 antibody, EF-12 antibody, Oit5 antibody, RGD1566416 antibody, dok-7 antibody, docking protein 7 antibody, DOK7 antibody, dok7 antibody, Dok7 antibody
    背景
    The protein encoded by this gene is essential for neuromuscular synaptogenesis. The protein functions in aneural activation of muscle-specific receptor kinase, which is required for postsynaptic differentiation, and in the subsequent clustering of the acetylcholine receptor in myotubes. This protein can also induce autophosphorylation of muscle-specific receptor kinase. Mutations in this gene are a cause of familial limb-girdle myasthenia autosomal recessive, which is also known as congenital myasthenic syndrome type 1B. Alternative splicing results in multiple transcript variants.
    分子量
    52.9 kDa
    基因ID
    285489
    NCBI登录号
    NM_173660
    HGNC
    285489
    途径
    Skeletal Muscle Fiber Development
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