Receptor Accessory Protein 1 anticorps (AA 61-110)

N° du produit ABIN7230988

Cet anticorps Lapin Polyclonal détecte spécifiquement Receptor Accessory Protein 1 dans WB et ELISA. Il présente une réactivité avec des échantillons de Souris et Humain.

Aperçu rapide pour Receptor Accessory Protein 1 anticorps (AA 61-110) (ABIN7230988)

Antigène: Receptor Accessory Protein 1 (REEP1)

Reactivité: Souris, Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Receptor Accessory Protein 1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-Receptor Accessory Protein 1 anticorps

Épitope: AA 61-110

Fonction: Rabbit Anti-REEP1 Polyclonal Antibody

Specificité: The antibody detects endogenous levels of REEP1 protein

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

Immunogène: Synthesized peptide derived from part region of human REEP1 protein at AA range: 61-110

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur Receptor Accessory Protein 1

Antigène: Receptor Accessory Protein 1 (REEP1)

Autre désignation: REEP1

Sujet: Receptor expression-enhancing protein 1, Spastic paraplegia 31 proteinREEP1 encodes a mitochondrial protein that functions to enhance the cell surface expression of odorant receptors. Mutations in REEP1 cause spastic paraplegia autosomal dominant type 31, a neurodegenerative disorder. Alternative splicing results in multiple transcript variants.

Poids moléculaire: 22kD

ID gène: 65055

UniProt: Q9H902