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DOK7 抗体 (N-Term)

The 兔 多克隆 anti-DOK7 antibody is suitable to detect DOK7 in samples from 小鼠. It has been validated for WB.
产品编号 ABIN657491
发货至: 中国
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Quick Overview for DOK7 抗体 (N-Term) (ABIN657491)

抗原

See all DOK7 抗体
DOK7 (Docking Protein 7 (DOK7))

适用

  • 32
  • 22
  • 18
小鼠

宿主

  • 45
  • 4
  • 1
  • 1

克隆类型

  • 47
  • 4
多克隆

标记

  • 20
  • 4
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DOK7 antibody is un-conjugated

应用范围

  • 40
  • 19
  • 13
  • 13
  • 10
  • 7
  • 7
  • 4
  • 4
  • 3
  • 2
Western Blotting (WB)

克隆位点

RB32528
  • 抗原表位

    • 15
    • 7
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 26-55, N-Term

    纯化方法

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    免疫原

    This DOK7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 26-55 amino acids from the N-terminal region of human DOK7.

    亚型

    Ig Fraction
  • 应用备注

    WB: 1:1000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    储存方法

    DOK7 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    有效期

    6 months
  • 抗原

    DOK7 (Docking Protein 7 (DOK7))

    别名

    DOK7

    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

    53097

    基因ID

    285489

    NCBI登录号

    NP_001158145, NP_001243825, NP_775931

    UniProt

    Q18PE1

    途径

    Skeletal Muscle Fiber Development
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