PMP22 anticorps (AA 111-160)

N° du produit ABIN1533382

L’anticorps anti-PMP22 Polyclonal Lapin est utilisé pour la détection de PMP22 dans des échantillons de Humain, Rat et Souris. Il a été validé pour WB, IHC, ELISA et IF.

Aperçu rapide pour PMP22 anticorps (AA 111-160) (ABIN1533382)

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

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PMP22 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)

Détail du produit anti-PMP22 anticorps

Épitope: AA 111-160

Fonction: GAS3 Antibody

Specificité: GAS3 Polyclonal Antibody detects endogenous levels of GAS3 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Pureté: > 95 %

Immunogène: The antiserum was produced against synthesized peptide derived from human PMP22. AA range:111-160

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % 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: -20 °C

Stockage commentaire: Store at -20°C/1 year

Date de péremption: 12 months

Détails sur PMP22

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

Autre désignation: PMP22

Sujet:

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

Background: This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Studies suggest two alternately used promoters drive tissue-specific expression. 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. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013],

Gene Name: PMP22

Protein Name: Peripheral myelin protein 22

Poids moléculaire: 17 kDa

ID gène: 5376

OMIM: 601097

UniProt: Q01453