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PMP22 anticorps

Cet anticorps anti-PMP22 est un anticorps Lapin Polyclonal détectant PMP22 dans WB et EIA. Adapté pour Humain.
N° du produit ABIN954219

Aperçu rapide pour PMP22 anticorps (ABIN954219)

Antigène

Voir toutes PMP22 Anticorps
PMP22 (Peripheral Myelin Protein 22 (PMP22))

Reactivité

  • 46
  • 42
  • 32
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 58
  • 7
Lapin

Clonalité

  • 50
  • 15
Polyclonal

Conjugué

  • 25
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp PMP22 est non-conjugé

Application

  • 46
  • 20
  • 14
  • 14
  • 13
  • 8
  • 7
  • 6
  • 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
  • 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

    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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