PEX3 anticorps (AA 12-61)

N° du produit ABIN1535149

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

Aperçu rapide pour PEX3 anticorps (AA 12-61) (ABIN1535149)

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), Immunohistochemistry (IHC), ELISA

Détail du produit anti-PEX3 anticorps

Épitope: AA 12-61

Fonction: Peroxin 3 Antibody

Specificité: Peroxin 3 Polyclonal Antibody detects endogenous levels of Peroxin 3 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 PEX3. AA range:12-61

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-2000,IHC 1:50-300, ELISA 2000-20000

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 PEX3

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

Autre désignation: PEX3

Sujet:

Synonyms: PEX3, Peroxisomal biogenesis factor 3, Peroxin-3, Peroxisomal assembly protein 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). [provided by RefSeq, Oct 20

Gene Name: PEX3

Protein Name: Peroxisomal biogenesis factor 3

Poids moléculaire: 42 kDa

ID gène: 8504

OMIM: 214100

UniProt: P56589