PEX12 anticorps

N° du produit ABIN7258886

Détail du produit anti-PEX12 anticorps

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX12 est non-conjugé

Application: Western Blotting (WB)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein 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

Concentration: 1 mg/mL

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 (PEX12 Produits)

Synonymes: anticorps zgc:56182, anticorps pex12, anticorps MGC81372, anticorps PEX12, anticorps DDBDRAFT_0186545, anticorps DDBDRAFT_0238076, anticorps DDB_0186545, anticorps DDB_0238076, anticorps LOC100226224, anticorps PAF-3, anticorps PBD3A, anticorps Peroxin-12, anticorps AI451906, anticorps peroxisomal biogenesis factor 12, anticorps peroxisomal biogenesis factor 12 L homeolog, anticorps RING zinc finger-containing protein, anticorps pex12, anticorps PEX12, anticorps pex12.L, anticorps 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).

Poids moléculaire:

Observed_MW: 41 kDa

Calculated_MW: 40 kDa

ID gène: 5193

UniProt: O00623