PEX10 anticorps (AA 1-100)

N° du produit ABIN6989470

Cet anticorps Lapin Polyclonal détecte spécifiquement PEX10 dans IF (cc), IF (p), IHC (p) et IHC (fro). Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour PEX10 anticorps (AA 1-100) (ABIN6989470)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX10 est non-conjugé

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-PEX10 anticorps

Épitope: AA 1-100

Fonction: PEX10 Polyclonal Antibody

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: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Stockage commentaire: Shipped at 4C. Store at -20C for one year. 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