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PMP22 anticorps (AA 102-130)

Cet anticorps anti-PMP22 est un anticorps Lapin Polyclonal détectant PMP22 dans WB. Adapté pour Humain.
N° du produit ABIN5531914

Aperçu rapide pour PMP22 anticorps (AA 102-130) (ABIN5531914)

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
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 15
    • 6
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 102-130

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This PMP22 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 102-130 amino acids from human PMP22.

    Isotype

    Ig Fraction
  • Indications d'application

    For WB starting dilution is: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    Supplied in PBS with 0.09 % (W/V) sodium azide.

    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.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • 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.

    Poids moléculaire

    18 kDa

    ID gène

    5376

    UniProt

    Q01453
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