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MPZ antibody

This anti-MPZ antibody is a Rabbit Polyclonal antibody detecting MPZ in WB. Suitable for Human.
Catalog No. ABIN1513218
-15% Promotion 2026
$301.75
$355.00
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Quick Overview for MPZ antibody (ABIN1513218)

Target

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

Reactivity

  • 41
  • 28
  • 25
  • 15
Human

Host

  • 49
  • 7
  • 3
  • 1
Rabbit

Clonality

  • 53
  • 7
Polyclonal

Conjugate

  • 28
  • 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

Application

  • 49
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  • 13
  • 13
  • 7
  • 7
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  • 1
Western Blotting (WB)
  • Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant protein of human MPZ

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

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

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid freeze / thaw cycles

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    MPZ (Myelin Protein Zero (MPZ))

    Alternative Name

    MPZ

    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.,MPZ,CHM,CMT1,CMT1B,CMT2I,CMT2J,CMT4E,CMTDI3,CMTDID,DSS,HMSNIB,MPP,P0,Neuroscience,Cell Type Marker,Neurodegenerative Diseases,Neuron marker,Axon marker,MPZ

    Molecular Weight

    27 kDa/34 kDa

    Gene ID

    4359

    UniProt

    P25189
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