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MPZ 抗体 (AA 50-130)

The 兔 多克隆 anti-MPZ antibody (ABIN8123104) specifically detects MPZ in WB 和 ELISA. The antibody is reactive with 人, 大鼠 和 小鼠 samples.
产品编号 ABIN8123104
发货至: 中国
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Quick Overview for MPZ 抗体 (AA 50-130) (ABIN8123104)

抗原

See all MPZ 抗体
MPZ (Myelin Protein Zero (MPZ))

适用

人, 大鼠, 小鼠

宿主

  • 60
  • 15
  • 3
  • 1
兔

克隆类型

  • 64
  • 15
多克隆

标记

  • 37
  • 6
  • 5
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MPZ antibody is un-conjugated

应用范围

  • 59
  • 31
  • 24
  • 13
  • 13
  • 11
  • 5
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), ELISA
  • 抗原表位

    • 15
    • 12
    • 6
    • 5
    • 5
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    AA 50-130

    原理

    MYP0 Antibody

    特异性

    MYP0 Polyclonal Antibody detects endogenous levels of protein.

    纯化方法

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    免疫原

    Synthesized peptide derived from human protein . at AA range: 50-130

    亚型

    IgG
  • 应用备注

    WB 1:500-2000 ELISA 1:5000-20000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Liquid in PBS containing 50 % glycerol, and 0.02 % 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

    -20 °C

    储存方法

    Store at -20°C/1 year

    有效期

    12 months
  • 抗原

    MPZ (Myelin Protein Zero (MPZ))

    别名

    MYP0

    背景

    Background: This gene is specifically expressed in Schwann cells of the peripheral nervous system and encodes a type I transmembrane glycoprotein that is a major structural protein of the peripheral myelin sheath. The encoded protein contains a large hydrophobic extracellular domain and a smaller basic intracellular domain, which are essential for the formation and stabilization of the multilamellar structure of the compact myelin. Mutations in this gene are associated with autosomal dominant form of Charcot-Marie-Tooth disease type 1 (CMT1B) and other polyneuropathies, such as Dejerine-Sottas syndrome (DSS) and congenital hypomyelinating neuropathy (CHN). A recent study showed that two isoforms are produced from the same mRNA by use of alternative in-frame translation termination codons via a stop codon readthrough mechanism. [provided by RefSeq, Oct 2015],

    Gene Name: MPZ

    Protein Name: Myelin protein P0 (Myelin peripheral protein) (MPP) (Myelin protein zero)

    基因ID

    4359

    UniProt

    P25189
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