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DOK7 Protein (Myc-DYKDDDDK Tag)

DOK7 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2719665
发货至: 中国
  • 抗原 See all DOK7 蛋白
    DOK7 (Docking Protein 7 (DOK7))
    蛋白类型
    Recombinant
    宿主
    • 1
    • 1
    • 1
    资源
    • 2
    • 1
    HEK-293 Cells
    标记
    This DOK7 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human DOK7 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product DOK7 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    储存条件
    -80 °C
    储存方法
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原
    DOK7 (Docking Protein 7 (DOK7))
    别名
    Dok7 (DOK7 产品)
    别名
    si:dkey-180b4.3 Protein, si:ch211-164d19.2 Protein, C4orf25 Protein, CMS1B Protein, A930013K19Rik Protein, AW049091 Protein, Dok-7 Protein, EF-12 Protein, Oit5 Protein, RGD1566416 Protein, dok-7 Protein, docking protein 7 Protein, DOK7 Protein, dok7 Protein, Dok7 Protein
    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
    NCBI登录号
    NP_775931
    途径
    Skeletal Muscle Fiber Development
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