PEX10 anticorps (Middle Region)

N° du produit ABIN2781270

L’anticorps Lapin Polyclonal anti-PEX10 a été validé pour WB et IHC. Il convient pour détecter PEX10 dans des échantillons de Humain.

Aperçu rapide pour PEX10 anticorps (Middle Region) (ABIN2781270)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX10 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Détail du produit anti-PEX10 anticorps

Épitope: Middle Region

Séquence: QALRPDPLRV LMSVAPSALQ LRVRSLPGED LRARVSYRLL GVISLLHLVL

Homologie: Human: 100%

Attributs du produit: This is a rabbit polyclonal antibody against PEX10. It was validated on Western Blot and immunohistochemistry.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the middle region of human PEX10

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator.

Commentaires:

Antigen size: 346 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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.

Conseil sur la manipulation: Avoid repeated freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur PEX10

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

Autre désignation: 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.
Alias Symbols: MGC1998, NALD, RNF69
Protein Interaction Partner: HNRNPD, PEX5, PEX14, LIG4, PCGF6, CGRRF1, MKRN3, PEX19, PEX12, PEX10, UBC, UBE2I, PEX2,
Protein Size: 346

Poids moléculaire: 39 kDa

ID gène: 5192

NCBI Accession: NM_153818, NP_722540

Pathways: Monocarboxylic Acid Catabolic Process