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XPA 抗体 (full length)

This anti-XPA antibody is a 小鼠 单克隆 antibody detecting XPA in WB, ELISA 和 Inhibition. Suitable for 人. This Primary Antibody has been cited in 2+ publications.
产品编号 ABIN3200998
发货至: 中国

Quick Overview for XPA 抗体 (full length) (ABIN3200998)

抗原

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

适用

  • 48
  • 16
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1

宿主

  • 44
  • 4
小鼠

克隆类型

  • 46
  • 2
单克隆

标记

  • 31
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This XPA antibody is un-conjugated

应用范围

  • 38
  • 20
  • 12
  • 8
  • 7
  • 6
  • 5
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Blocking Antibody (Inhibition)

克隆位点

5F12
  • 抗原表位

    • 8
    • 8
    • 8
    • 7
    • 5
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    full length

    交叉反应

    小鼠

    交叉反应 (详细)

    Expected to react also with mouse XPA from the sequence homology.

    纯化方法

    Purified

    过滤

    Sterile filtered

    免疫原

    Recombinant full-length human XPA protein

    亚型

    IgG2b
  • 应用备注

    1. Western blotting: 0. 1~1 g/mL
    2. ELISA
    3. Inhibition of in vitro excision repair reaction
    4. Inhibition of XPA interaction with ERCC1 and TFIIH
    Other applications have not been tested.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS pH 7.2, 50 % glycerol

    储存液

    Azide free

    储存条件

    -20 °C/-80 °C

    储存方法

    -20 C (For long term storage: -70 C)
  • Saijo, Matsuda, Kuraoka, Tanaka: "Inhibition of nucleotide excision repair by anti-XPA monoclonal antibodies which interfere with binding to RPA, ERCC1, and TFIIH." in: Biochemical and biophysical research communications, Vol. 321, Issue 4, pp. 815-22, (2004) (PubMed).

    Tanaka, Miura, Satokata, Miyamoto, Yoshida, Satoh, Kondo, Yasui, Okayama, Okada: "Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain." in: Nature, Vol. 348, Issue 6296, pp. 73-6, (1990) (PubMed).

  • 抗原

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

    别名

    XPA

    背景

    XP (Xeroderma pigmentosum) is an autosomal recessive human disease characterized by hypersensitivity to sunlight and a high incidence of skin cancer on sun-exposed skin. Cells from XP patients are hypersensitive to killing by UV irradiation because of a defect in nucleotide excision repair (NER). XP is classified into seven complementation groups (A~G) and a variant form. XPA shows the most severe symptoms. Products encoded by the XP genes function in repairing UV-induced cyclobutane pyrimidine dimmer and (6-4) photoproducts as well as chemically induced variety of DNA lesions. XPA protein consists of 273 amino acids and forms a complex with many proteins such as RPA, ERCC1, TFIIH,XAB1, and XAB2, which plays a role in early step of NER. The hybridoma 5F12 was constructed by Prof. K. Tanaka's group who first cloned the XPA gene.

    UniProt

    P23025

    途径

    DNA Damage Repair
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