PEX10 anticorps (AA 1-100) (HRP)

N° du produit ABIN6987473

L’anticorps Lapin Polyclonal anti-PEX10 a été validé pour ELISA, IHC (p) et IHC (fro). Il convient pour détecter PEX10 dans des échantillons de Souris.

Aperçu rapide pour PEX10 anticorps (AA 1-100) (HRP) (ABIN6987473)

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

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX10 est conjugé à/à la HRP

Application: ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-PEX10 anticorps (HRP)

Épitope: AA 1-100

Réactivité croisée: Souris

Homologie: Human,Rat,Cow

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human PEX10

Isotype: IgG

Information d'application

Indications d'application: IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur PEX10

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

Autre désignation: PEX10

Sujet:

Synonyms: AV128229, Gm142, MGC1998, NALD, OTTHUMP00000001658, PBD6A, PBD6B, peroxin 10, Peroxin-10, Peroxisomal biogenesis factor 10, Peroxisome assembly protein 10, Peroxisome biogenesis factor 10, PEX10, PEX10_HUMAN, RING finger protein 69, RNF69, RP23-298E4.1.

Background: 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. [provided by RefSeq, Jul 2008]

ID gène: 5192

UniProt: O60683

Pathways: Monocarboxylic Acid Catabolic Process