PEX10 anticorps

N° du produit ABIN2458699

Détail du produit anti-PEX10 anticorps

Antigène: PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX10 est non-conjugé

Application: Western Blotting (WB), ELISA

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human PEX10.

Information d'application

Indications d'application: PEX10 antibody can be used for detection of PEX10 by ELISA at 1:1562500. PEX10 antibody can be used for detection of PEX10 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

Stockage commentaire: For short periods of storage (days) store at 4 °C. For longer periods of storage, store PEX10 antibody at -20 °C.

Détails sur PEX10

Antigène: PEX10 (Peroxisomal Biogenesis Factor 10 (PEX10))

Autre désignation: PEX10 (PEX10 Produits)

Synonymes: anticorps ATPEX10, anticorps T9J22.2, anticorps peroxin 10, anticorps NALD, anticorps PBD6A, anticorps PBD6B, anticorps RNF69, anticorps AV128229, anticorps Gm142, anticorps peroxin 10, anticorps peroxisomal biogenesis factor 10, anticorps PEX10, anticorps Pex10

Sujet: PEX10 is a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in PEX10 gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome.This gene encodes a protein involved in import of peroxisomal matrix proteins. This protein localizes to the peroxisomal membrane. Mutations in this gene result in phenotypes within the Zellweger spectrum of peroxisomal biogenesis disorders, ranging from neonatal adrenoleukodystrophy to Zellweger syndrome. Alternative splicing results in two transcript variants encoding different isoforms.

Poids moléculaire: 37 kDa

ID gène: 5192

NCBI Accession: NP_002608

UniProt: O60683

Pathways: Monocarboxylic Acid Catabolic Process