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MPZ 抗体 (full length)

The 小鼠 单克隆 anti-MPZ antibody is suitable to detect MPZ in samples from 人. It has been validated for IHC (p).
产品编号 ABIN7878681
发货至: 中国
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Quick Overview for MPZ 抗体 (full length) (ABIN7878681)

抗原

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

适用

  • 48
  • 28
  • 25
  • 15

宿主

  • 49
  • 14
  • 3
  • 1
小鼠

克隆类型

  • 53
  • 14
单克隆

标记

  • 35
  • 5
  • 4
  • 4
  • 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

  • 49
  • 25
  • 24
  • 13
  • 13
  • 10
  • 7
  • 7
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

质量等级

Carrier-free

克隆位点

MPZ-7390
  • 抗原表位

    • 15
    • 6
    • 5
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    full length

    原理

    MPZ Antibody / Myelin Protein Zero (azide and preservative free)

    纯化方法

    Protein A/G affinity

    免疫原

    Recombinant full-length human MPZ protein was used as the immunogen for the MPZ antibody.

    亚型

    IgG2a, kappa
  • 应用备注

    Optimal dilution of the MPZ antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    储存液

    Azide free

    储存条件

    -20 °C

    储存方法

    Aliquot the MPZ antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • 抗原

    MPZ (Myelin Protein Zero (MPZ))

    别名

    MPZ

    背景

    Zero, also known as myelin protein zero (MPZ) is a Type 1 integral membrane glycoprotein that mediates adhesion of spiraling wraps of the myelin sheath in order to ensure stable synaptic transmission. Zero protein encompasses approximately 50 % of total protein in the sheath scaffolding in contribution to structural integrity of peripheral myelin. Zero guides the compact myelin wrapping process through glycine zipper packing interface-dependent dimer and tetramer formation. Mutations (e.g. G134R) can abrogate multimer formation, cause demyelinating neuropathies, and are known to contribute to conditions that include Charcot-Marie-Tooth disease. Zero cytoplasmic domain undergoes serine and tyrosine phosphorylation, which appears to be prevalent during peak nerve myelination. Zero transcript is moderate in brain, abundant in thymus and most abundant in white matter of the CNS.

    UniProt

    P25189
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