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BZW2 抗体 (AA 21-292)

This 兔 多克隆 antibody specifically detects BZW2 in WB, ELISA, IHC (p) 和 FACS. It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN7872158
发货至: 中国
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Quick Overview for BZW2 抗体 (AA 21-292) (ABIN7872158)

抗原

See all BZW2 抗体
BZW2 (Basic Leucine Zipper and W2 Domains 2 (BZW2))

适用

  • 33
  • 21
  • 20
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
人, 小鼠, 大鼠

宿主

  • 31
  • 2

克隆类型

  • 33
多克隆

标记

  • 13
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This BZW2 antibody is un-conjugated

应用范围

  • 26
  • 13
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • 抗原表位

    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 21-292

    原理

    BZW2 Antibody / eIF5-mimic protein 1

    纯化方法

    Antigen affinity purified

    免疫原

    Recombinant human protein (amino acids E21-A292) was used as the immunogen for the BZW2 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the BZW2 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 BZW2 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

    BZW2 (Basic Leucine Zipper and W2 Domains 2 (BZW2))

    别名

    BZW2

    背景

    Basic Leucine Zipper and W2 Domain-Containing Protein 2 is a protein that is encoded by the BZW2 gene. BZW2, also known as HSPC028 or MSTP017, is a 419 amino acid protein that contains one W2 domain and is thought to be involved in neuronal differentiation. The gene encoding BZW2 maps to human chromosome 7. Chromosome 7 houses over 1,000 genes and comprises nearly 5 % of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders, including cases of acute myelogenous leukemia and myelodysplasia.

    UniProt

    Q9Y6E2

    途径

    SARS-CoV-2 Protein Interactome
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