PMP22 monoclonal antibody, clone Hu1

Catalog # MAB2301

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Size:100 uL
Price: USD $ 531.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Application

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

Immunohistochemical staining of PMP22 on formalin fixed, paraffin embedded dorsal root ganglion and spinal roots in 20 week fetal spinal cord preparation from rhesus monkey with PMP22 monoclonal antibody, clone Hu1 (Cat # MAB2301).

  • Specification

    Product Description

    Mouse monoclonal antibody raised against synthetic peptide of PMP22.

    Immunogen

    A synthetic peptide corresponding to amino acids 120-133 at the extracellular domain of human PMP22.

    Host

    Mouse

    Reactivity

    Human, Primates

    Form

    Liquid

    Isotype

    IgG1, kappa

    Quality Control Testing

    Antibody Reactive Against Synthetic Peptide.

    Recommend Usage

    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In Tris-glycine, 150 mM NaCl (0.05% sodium azide)

    Storage Instruction

    Store at -20°C or -80°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

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

  • Applications

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

    Immunohistochemical staining of PMP22 on formalin fixed, paraffin embedded dorsal root ganglion and spinal roots in 20 week fetal spinal cord preparation from rhesus monkey with PMP22 monoclonal antibody, clone Hu1 (Cat # MAB2301).
  • Gene Info — PMP22

    Entrez GeneID

    5376

    Protein Accession#

    Q01453

    Gene Name

    PMP22

    Gene Alias

    CMT1A, CMT1E, DSS, GAS-3, HMSNIA, HNPP, MGC20769, Sp110

    Gene Description

    peripheral myelin protein 22

    Omim ID

    118220 118300 145900 162500 180800 601097

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing of this gene results in three transcript variants that encode the same protein. [provided by RefSeq

    Other Designations

    growth arrest-specific 3

  • Interactome
  • Disease
  • Publication Reference
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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