PEX12 anticorps (Middle Region)

N° du produit ABIN954095

L’anticorps anti-PEX12 Polyclonal Lapin est utilisé pour la détection de PEX12 dans des échantillons de Humain et Souris. Il a été validé pour WB et EIA.

Aperçu rapide pour PEX12 anticorps (Middle Region) (ABIN954095)

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX12 est non-conjugé

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Détail du produit anti-PEX12 anticorps

Épitope: AA 137-167, Middle Region

Specificité: This antibody recognizes Human and Mouse Peroxin 12 / PEX12 (Center).

Purification: Protein A column, followed by peptide affinity purification

Immunogène: KLH conjugated synthetic peptide between 137~167 amino acids from the Central region of human PEX12

Isotype: Ig Fraction

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

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 freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur PEX12

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

Autre désignation: Peroxin 12 / 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.Synonyms: PAF-3, PAF3, Peroxin-12, Peroxisome assembly factor 3, Peroxisome assembly protein 12

Poids moléculaire: 40797 Da

ID gène: 5193

NCBI Accession: NP_000277