PEX12 anticorps (AA 290-359)

N° du produit ABIN7269246

Cet anticorps anti-PEX12 Polyclonal Lapin (ABIN7269246) détecte spécifiquement PEX12 dans WB. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour PEX12 anticorps (AA 290-359) (ABIN7269246)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX12 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-PEX12 anticorps

Épitope: AA 290-359

Fonction: PEX12 Rabbit pAb

Séquence: YNSDSPLLPK MKTVCPLCRK TRVNDTVLAT SGYVFCYRCV FHYVRSHQAC PITGYPTEVQ HLIKLYSPEN

Réactivité croisée: Humain

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 290-359 of human PEX12 (NP_000277.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,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.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur PEX12

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

Autre désignation: PEX12

Sujet: This gene belongs to the peroxin-12 family. 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 of Zellweger syndrome (ZWS).,PEX12,PAF-3,PBD3A,Signal Transduction,PEX12

Poids moléculaire: 40kDa

ID gène: 5193

UniProt: O00623