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NUB1 抗体 (AA 190-543)

The 兔 多克隆 anti-NUB1 antibody (ABIN7871644) specifically detects NUB1 in WB, ELISA, IHC (p), IF 和 FACS. The antibody is reactive with 人, 小鼠, 猴 和 大鼠 samples.
产品编号 ABIN7871644
发货至: 中国
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Quick Overview for NUB1 抗体 (AA 190-543) (ABIN7871644)

抗原

See all NUB1 抗体
NUB1 (Negative Regulator of Ubiquitin-Like Proteins 1 (NUB1))

适用

  • 39
  • 16
  • 5
  • 3
  • 1
人, 小鼠, 猴, 大鼠

宿主

  • 34
  • 5

克隆类型

  • 36
  • 3
多克隆

标记

  • 22
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This NUB1 antibody is un-conjugated

应用范围

  • 32
  • 22
  • 20
  • 8
  • 6
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF), Flow Cytometry (FACS)
  • 抗原表位

    • 8
    • 7
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 190-543

    原理

    NUB1 Antibody / NEDD8 ultimate buster 1 / NYREN18

    纯化方法

    Antigen affinity purified

    免疫原

    An E.coli-derived human recombinant protein (K190-D543) was used as the immunogen for the NUB1 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the NUB1 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the NUB1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    NUB1 (Negative Regulator of Ubiquitin-Like Proteins 1 (NUB1))

    别名

    NUB1

    背景

    NEDD8 µLtimate buster 1 is a protein that in humans is encoded by the NUB1 gene. This gene encodes a protein that functions as a negative regulator of NEDD8, a ubiquitin-like protein that conjugates with cullin family members in order to regulate vital biological events. The protein encoded by this gene regulates the NEDD8 conjugation system post-transcriptionally by recruiting NEDD8 and its conjugates to the proteasome for degradation. This protein interacts with the product of the AIPL1 gene, which is associated with Leber congenital amaurosis, an inherited retinopathy, and mutations in that gene can abolish interaction with this protein, which may contribute to the pathogenesis. This protein is also known to accumulate in Lewy bodies in Parkinson's disease and dementia with Lewy bodies, and in glial cytoplasmic inclusions in multiple system atrophy, with this abnormal accumulation being specific to alpha-synucleinopathy lesions. Alternative splicing of this gene results in multiple transcript variants.

    UniProt

    Q9Y5A7
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