PEX3 anticorps

N° du produit ABIN7117349

L’anticorps Lapin Polyclonal anti-PEX3 a été validé pour WB, ELISA et IHC. Il convient pour détecter PEX3 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour PEX3 anticorps (ABIN7117349)

Antigène: PEX3 (Peroxisomal Biogenesis Factor 3 (PEX3))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX3 est non-conjugé

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

Détail du produit anti-PEX3 anticorps

Fonction: PEX3 antibody

Purification: Immunogen affinity purified

Pureté: ≥95 % as determined by SDS-PAGE

Immunogène: peroxisomal biogenesis factor 3

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500 - 1:2000, IHC: 1:50 - 1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

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.

Conseil sur la manipulation: Avoid repeated freeze / thaw cycles.

Stock: -20 °C

Stockage commentaire: -20°C for 12 months

Date de péremption: 12 months

Détails sur PEX3

Antigène: PEX3 (Peroxisomal Biogenesis Factor 3 (PEX3))

Autre désignation: PEX3

Sujet:

Synonyms: Peroxisomal biogenesis factor 3|Peroxin-3|Peroxisomal assembly protein PEX3|PEX3

Background: The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause Zellweger syndrome (ZWS).

Poids moléculaire: 37 kDa

ID gène: 8504

UniProt: P56589