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PMP22 anticorps

PMP22 Reactivité: Humain WB, EIA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN954219
  • Antigène Voir toutes PMP22 Anticorps
    PMP22 (Peripheral Myelin Protein 22 (PMP22))
    Reactivité
    • 48
    • 42
    • 33
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 59
    • 7
    Lapin
    Clonalité
    • 51
    • 15
    Polyclonal
    Conjugué
    • 25
    • 4
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp PMP22 est non-conjugé
    Application
    • 46
    • 20
    • 14
    • 14
    • 12
    • 9
    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Enzyme Immunoassay (EIA)
    Specificité
    This antibody recognizes Human PMP22
    Purification
    Protein A column, followed by peptide affinity purification
    Immunogène
    KLH conjugated synthetic peptide selected from 110-140 Human PMP22. Genename: PMP22
    Isotype
    Ig Fraction
    Top Product
    Discover our top product PMP22 Anticorps primaire
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.25 mg/mL
    Buffer
    PBS containing 0.09 % (W/V) Sodium Azide as preservativee
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Conseil sur la manipulation
    Avoid repeated freezing and thawing.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Antigène
    PMP22 (Peripheral Myelin Protein 22 (PMP22))
    Autre désignation
    PMP22 (PMP22 Produits)
    Sujet
    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.Synonyms: GAS-3, GAS3, Growth arrest-specific protein 3, PMP-22, Peripheral myelin protein 22
    Poids moléculaire
    17891 Da
    ID gène
    5376
    NCBI Accession
    NP_696996
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