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PDCD10 抗体 (AA 96-124)

This anti-PDCD10 antibody is a 兔 多克隆 antibody detecting PDCD10 in WB. Suitable for 人.
产品编号 ABIN1538712
发货至: 中国

Quick Overview for PDCD10 抗体 (AA 96-124) (ABIN1538712)

抗原

See all PDCD10 抗体
PDCD10 (Programmed Cell Death 10 (PDCD10))

适用

  • 42
  • 28
  • 14

宿主

  • 55
  • 2

克隆类型

  • 55
  • 2
多克隆

标记

  • 19
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PDCD10 antibody is un-conjugated

应用范围

  • 22
  • 20
  • 13
  • 13
  • 6
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB)

克隆位点

RB21118
  • 抗原表位

    • 15
    • 11
    • 6
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 96-124

    预测反应

    Zf, C, M, Rat, X

    纯化方法

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    免疫原

    This PDCD10 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 96-124 amino acids from the Central region of human PDCD10.

    亚型

    Ig Fraction
  • 应用备注

    WB: 1:1000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    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

    4 °C,-20 °C

    储存方法

    PDCD10 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    有效期

    6 months
  • 抗原

    PDCD10 (Programmed Cell Death 10 (PDCD10))

    别名

    PDCD10

    背景

    This gene encodes an evolutionarily conserved protein associated with cell apoptosis. The protein interacts with the serine/threonine protein kinase MST4 to modulate the extracellular signal-regulated kinase (ERK) pathway. It also interacts with and is phosphoryated by serine/threonine kinase 25, and is thought to function in a signaling pathway essential for vascular developent. Mutations in this gene are one cause of cerebral cavernous malformations, which are vascular malformations that cause seizures and cerebral hemorrhages. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq].

    分子量

    24702

    基因ID

    11235

    NCBI登录号

    NP_009148, NP_665858, NP_665859

    UniProt

    Q9BUL8
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