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XPA 抗体

This 兔 多克隆 antibody specifically detects XPA in WB 和 IHC (p). It exhibits reactivity toward 人 和 小鼠.
产品编号 ABIN271978
发货至: 中国
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Quick Overview for XPA 抗体 (ABIN271978)

抗原

See all XPA 抗体
XPA (Xeroderma Pigmentosum, Complementation Group A (XPA))

适用

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  • 1
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  • 1
人, 小鼠

宿主

  • 45
  • 6

克隆类型

  • 47
  • 4
多克隆

标记

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  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
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This XPA antibody is un-conjugated

应用范围

  • 41
  • 24
  • 12
  • 12
  • 6
  • 6
  • 5
  • 4
  • 2
  • 1
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  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 特异性

    This antibody detects endogenous levels of XPA protein. (region surrounding His244)

    交叉反应 (详细)

    Species reactivity (tested):Human and Mouse.

    纯化方法

    Affinity Chromatography using epitope-specific immunogen.
  • 应用备注

    ELISA: 1/5000approx. 1/10000. Western blot: 1/500approx. 1/1000. Immunohistochemistry: 1/50approx. 1/200.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.

    限制

    仅限研究用
  • 浓度

    1.0 mg/mL

    缓冲液

    Phosphate buffered saline (PBS), pH 7.2., 0.05 % 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.

    注意事项

    Avoid repeated freezing and thawing.

    储存条件

    4 °C/-20 °C

    储存方法

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • 抗原

    XPA (Xeroderma Pigmentosum, Complementation Group A (XPA))

    别名

    XPA / XPAC

    背景

    Xeroderma pigmentosum (XP) is an autosomal recessive disorder characterized by a genetic predisposition to sunlight-induced skin cancer due to deficiencies in the DNA repair enzymes. The most frequent mutations are found in the XP genes of group A through G and group V, which encode nucleotide excision repair proteins. The XPA gene encodes a 31 kDa zinc metalloprotein that preferentially binds to DNA damaged by UV radiation and chemical carcinogens and is required for the incision step during nucleotide excision repair. The XPB and XPD genes encode DNA helicases involved in several DNA metabolic pathways, including DNA repair and transcription, and the XPG gene product is an endonuclease that cuts on the 3' side of a DNA lesion during nucleotide excision repair. Molecular defects in the XP variant (XPV) group maintain normal excision repair, yet they result in a substantial reduction in the ability to synthesize intact daughter DNA strands during DNA replication following DNA damage.Synonyms: DNA repair protein complementing XP-A cells, Xeroderma pigmentosum group A-complementing protein

    分子量

    approx. 33, 40 kDa

    基因ID

    7507

    NCBI登录号

    NP_000371

    UniProt

    P23025

    途径

    DNA Damage Repair
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