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TDP1 抗体 (AA 75-125)

This anti-TDP1 antibody is a 兔 多克隆 antibody detecting TDP1 in IP. Suitable for 人.
产品编号 ABIN7452451
发货至: 中国

Quick Overview for TDP1 抗体 (AA 75-125) (ABIN7452451)

抗原

See all TDP1 抗体
TDP1 (Tyrosyl-DNA Phosphodiesterase 1 (TDP1))

适用

  • 36
  • 17
  • 6
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1

宿主

  • 32
  • 6
  • 1

克隆类型

  • 35
  • 4
多克隆

标记

  • 30
  • 2
  • 2
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  • 1
  • 1
  • 1
This TDP1 antibody is un-conjugated

应用范围

  • 33
  • 17
  • 12
  • 10
  • 7
  • 7
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
Immunoprecipitation (IP)
  • 抗原表位

    • 7
    • 6
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 75-125

    原理

    Rabbit anti-TDP1 Antibody, Affinity Purified

    纯化方法

    Affinity Purified

    免疫原

    between AA 75 and 125

    亚型

    IgG
  • 应用备注

    IP: 2 - 5 μg/mg lysate

    WB: Not recommended. Use rabbit anti-TDP1 antibody ABIN7453800.

    限制

    仅限研究用
  • 浓度

    1000 μg/mL

    缓冲液

    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % 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

    有效期

    12 months
  • 抗原

    TDP1 (Tyrosyl-DNA Phosphodiesterase 1 (TDP1))

    别名

    TDP1

    背景

    Background: Tyrosyl-DNA phosphodiesterase 1 (TDP1) is an enzyme that participates in the repair of DNA strand breaks associated with topoisomerase 1 (Top1) complexes. TDP1 catalyzes the removal of Top1 from DNA via the hydrolysis of the phosphodiester bond between the tyrosine residue of Top1 and the 3' phosphate of DNA. Removal of Top1 is then followed by DNA repair. TDP1 has been proposed to play more general roles in DNA damage repair independent of the Top1 complex. TDP1 has been shown to associate with DNA ligase IIIalpha, a component of the DNA single-stranded break repair (SSBR) machinery. It is also able to remove glycolate from 3'-phosphoglycolate termini of double-stranded breaks and a variety of other 3'- adducts. Defects in TDP1 are associated with spinocerebellar ataxia autosomal recessive with axonal neuropathy (SCAN1), a disease associated with peripheral axonal motor and sensory neuropathy and distal muscular atrophy.

    基因ID

    55775

    NCBI登录号

    NP_001008744

    UniProt

    Q9NUW8
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