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TRAP1 抗体 (AA 618-704)

This 兔 多克隆 antibody specifically detects TRAP1 in WB, ELISA 和 FACS. It exhibits reactivity toward 人, 大鼠 和 小鼠.
产品编号 ABIN7876142
发货至: 中国
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Quick Overview for TRAP1 抗体 (AA 618-704) (ABIN7876142)

抗原

See all TRAP1 抗体
TRAP1 (TNF Receptor-Associated Protein 1 (TRAP1))

适用

  • 90
  • 35
  • 20
  • 4
  • 2
  • 1
人, 大鼠, 小鼠

宿主

  • 98
  • 7

克隆类型

  • 70
  • 34
多克隆

标记

  • 41
  • 8
  • 5
  • 5
  • 5
  • 5
  • 5
  • 5
  • 5
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TRAP1 antibody is un-conjugated

应用范围

  • 64
  • 37
  • 27
  • 24
  • 16
  • 14
  • 14
  • 13
  • 11
  • 5
  • 3
  • 2
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • 抗原表位

    • 15
    • 8
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 618-704

    原理

    HSP75 Antibody / TRAP-1

    纯化方法

    Antigen affinity purified

    免疫原

    Recombinant human protein (amino acids A618-H704) was used as the immunogen for the HSP75 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the HSP75 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 HSP75 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

    TRAP1 (TNF Receptor-Associated Protein 1 (TRAP1))

    别名

    HSP75

    背景

    Heat shock protein 75 kDa, mitochondrial is a protein that in humans is encoded by the TRAP1 gene. It is mapped to 16p13.3. This gene encodes a mitochondrial chaperone protein that is member of the heat shock protein 90 (HSP90) family. The encoded protein has ATPase activity and interacts with tumor necrosis factor type I. And this protein may function in regulating cellular stress responses. In addition, it was found that TRAP1 interacted with the N-terminal half of TNFR1. Also, TRAP1 interacted with the C-terminal ends of the proteins encoded by both multiple exostoses-causing genes, EXT1 and EXT2, but not with EXTL1 or EXTL3.

    UniProt

    Q12931
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