PMP22 anticorps (AA 102-130)

N° du produit ABIN5531914

Cet anticorps anti-PMP22 Polyclonal Lapin (ABIN5531914) détecte spécifiquement PMP22 dans WB. L’anticorps est réactif avec des échantillons de Humain.

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

Antigène: PMP22 (Peripheral Myelin Protein 22 (PMP22))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PMP22 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-PMP22 anticorps

Épitope: 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

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Stockage

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.

Détails sur PMP22

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