PEX12 anticorps (AA 131-158)

N° du produit ABIN653557

Cet anticorps Lapin Polyclonal détecte spécifiquement PEX12 dans WB. Il présente une réactivité envers Humain.

Aperçu rapide pour PEX12 anticorps (AA 131-158) (ABIN653557)

Antigène: PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX12 est non-conjugé

Application: Western Blotting (WB)

Clone: RB22647

Détail du produit anti-PEX12 anticorps

Épitope: AA 131-158

Homologie: B, M

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This PEX12 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 131-158 amino acids from the Central region of human PEX12.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur PEX12

Antigène: PEX12 (Peroxisomal Biogenesis Factor 12 (PEX12))

Autre désignation: PEX12

Sujet: 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.

Poids moléculaire: 40797

ID gène: 5193

NCBI Accession: NP_000277

UniProt: O00623