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MAPKBP1 抗体

This anti-MAPKBP1 antibody is a 兔 多克隆 antibody detecting MAPKBP1 in WB, IHC 和 ELISA. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN7116438
发货至: 中国

Quick Overview for MAPKBP1 抗体 (ABIN7116438)

抗原

See all MAPKBP1 抗体
MAPKBP1 (Mitogen-Activated Protein Kinase Binding Protein 1 (MAPKBP1))

适用

  • 7
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 6
  • 1

克隆类型

  • 7
多克隆

标记

  • 7
This MAPKBP1 antibody is un-conjugated

应用范围

  • 7
  • 2
  • 2
  • 2
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • 纯化方法

    Immunogen affinity purified

    纯度

    ≥95 % as determined by SDS-PAGE

    免疫原

    mitogen-activated protein kinase binding protein 1

    亚型

    IgG
  • 应用备注

    WB: 1:200 - 1:500, IHC: 1:50 - 1:100

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,

    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.

    储存条件

    -20 °C

    储存方法

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    有效期

    12 months
  • 抗原

    MAPKBP1 (Mitogen-Activated Protein Kinase Binding Protein 1 (MAPKBP1))

    别名

    MAPKBP1

    背景

    Synonyms:JNKBP1, KIAA0596 Background:MAP kinases play a significant role in many biological processes, including cell adhesion and spreading, cell differentiation and apoptosis. MAPKBP-1 (mitogen-activated protein kinase binding protein 1), also known as JNKBP-1, is a 1, 514 amino acid protein that contains twelve WD repeats. Induced by TRAF2 (TNF receptor-associated factor 2) and Tak1 (TGF-β-activated kinase 1), MAPKBP-1 is thought to act an adaptor protein for NFκB (nuclear factor κ-B) activation. MAPKBP-1 interacts with JNK3 and may promote TRAF2 polyubiquitination. MAPKBP-1 exists as six alternatively spliced variants and is encoded by a gene located on human chromosome 15. Human chromosome 15 houses over 700 genes and comprises nearly 3 % of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.

    分子量

    165 kDa

    基因ID

    23005

    UniProt

    O60336
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