Recombinant PMP22 anticorps

N° du produit ABIN6944620

L’anticorps anti-PMP22 Monoclonal Lapin est utilisé pour la détection de PMP22 dans des échantillons de Humain et Rat. Il a été validé pour WB.

Aperçu rapide pour Recombinant PMP22 anticorps (ABIN6944620)

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

Type d'anticorp: Recombinant Antibody

Reactivité: Humain, Rat

Hôte: Lapin

Clonalité: Monoclonal

Conjugué: Cet anticorp PMP22 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-PMP22 anticorps

Fonction: PMP22 Recombinant Antibody

Réactivité croisée: Humain, Rat

Purification: Purified by Protein A.

Immunogène: Full length protein

Isotype: IgG

Information d'application

Indications d'application: WB(1:300-5000)

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

Buffer: 0.01M TBS ( pH 7.4), 1 % BSA, 0.02 % Proclin 300, and 50 % Glycerol

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C for 12 months.

Date de péremption: 12 months

Détails sur PMP22

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

Autre désignation: PMP22

Sujet:

Synonyms: Peripheral myelin protein 22, Growth arrest-specific protein 3, PMP-22, GAS-3, PMP22, GAS3

Background: PMP22 is a 22 kDa glycoprotein expressed in the compact myelin of the peripheral nervous system. In the peripheral nervous system, PMP 22 is produced by myelinating Schwann cells and is coexpressed with the genes for myelin basic protein (MBP) during nerve development and regeneration. Alterations in the level of this protein cause several genetic human diseases. If the protein is duplicated, patients develop Charcot Marie Tooth disease. If one copy of the gene is deleted, they suffer from the inherited tendency to pressure palsies.

ID gène: 5376

UniProt: Q01453