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ube3a 抗体 (full length)

This 小鼠 单克隆 antibody specifically detects ube3a in IF 和 FACS. It exhibits reactivity toward 人.
产品编号 ABIN7879289
发货至: 中国
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Quick Overview for ube3a 抗体 (full length) (ABIN7879289)

抗原

See all ube3a 抗体
ube3a (Ubiquitin Protein Ligase E3A (ube3a))

适用

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  • 2
  • 2
  • 1
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宿主

  • 52
  • 12
小鼠

克隆类型

  • 48
  • 16
单克隆

标记

  • 38
  • 5
  • 3
  • 3
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  • 2
  • 1
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This ube3a antibody is un-conjugated

应用范围

  • 38
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  • 10
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  • 4
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  • 1
Immunofluorescence (IF), Flow Cytometry (FACS)

质量等级

Carrier-free

克隆位点

PCRP-UBE3A-1A2
  • 抗原表位

    • 15
    • 8
    • 5
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    full length

    原理

    Ubiquitin-protein ligase E3A Antibody / UBE3A (azide and preservative free)

    纯化方法

    Protein A/G affinity

    免疫原

    Recombinant full-length human UBE3A protein was used as the immunogen for the Ubiquitin-protein ligase E3A antibody.

    亚型

    IgG1
  • 应用备注

    Optimal dilution of the Ubiquitin-protein ligase E3A antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    储存液

    Azide free

    储存条件

    -20 °C

    储存方法

    Aliquot the Ubiquitin-protein ligase E3A antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • 抗原

    ube3a (Ubiquitin Protein Ligase E3A (ube3a))

    别名

    Ubiquitin-protein ligase E3A

    背景

    E6-associating protein (E6-AP), also designated ubiquitin protein ligase E3A (UBE3A), is a component of the ubiquitin-mediated proteolytic pathway that selectively targets proteins for degradation by the 26S Proteasome. Ubiquitin(Ub) is directly conjugated to protein substrates by the transfer of Ub from anE2 ubiquitin conjugating enzyme to the target protein. This conjugation is facilitated by the enzymatic activity of E3 ubiquitin ligase family members such asE6-AP. Several substrates of E6-AP have been identified and include the tumor suppressor protein p53 and the mammalian homolog of Rad23, HHR23A.Previous studies have indicated that E6-AP associates with the human papilloma virus E6 oncogene, which forms a complex with p53 and there by potentiates E6-AP mediated ubiquitination of p53. Genetic mutations that impair E6-AP activity result in the accumulation of p53 in the cytoplasm, and in many instances, these mutations are associated with the development of the rare neurodevelopmental disorder Angelman syndrome (AS), which is characterized by severe motor dysfunction and mental retardation.

    UniProt

    Q05086

    途径

    Intracellular Steroid Hormone Receptor Signaling Pathway
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