PEX1 anticorps (AA 1234-1283)

N° du produit ABIN1535160

Cet anticorps Lapin Polyclonal détecte spécifiquement PEX1 dans ELISA, IHC et IF. Il présente une réactivité avec des échantillons de Humain et Souris.

Aperçu rapide pour PEX1 anticorps (AA 1234-1283) (ABIN1535160)

Antigène: PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX1 est non-conjugé

Application: ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)

Détail du produit anti-PEX1 anticorps

Épitope: AA 1234-1283

Fonction: Peroxin 1 Antibody

Specificité: Peroxin 1 Polyclonal Antibody detects endogenous levels of Peroxin 1 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 PEX1. AA range:1234-1283

Isotype: IgG

Information d'application

Indications d'application: IHC 1:100 - 1:300. ELISA: 1:10000.. 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 PEX1

Antigène: PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

Autre désignation: PEX1

Sujet:

Synonyms: PEX1, Peroxisome biogenesis factor 1, Peroxin-1, Peroxisome biogenesis disorder protein 1

Background: This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2013],

Gene Name: PEX1

Protein Name: Peroxisome biogenesis factor 1

Poids moléculaire: 142 kDa

ID gène: 5189

OMIM: 602136

UniProt: O43933