PEX26 anticorps (AA 1-265)

N° du produit ABIN1885866

Cet anticorps anti-PEX26 Polyclonal Lapin (ABIN1885866) détecte spécifiquement PEX26 dans WB, IHC et IF. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour PEX26 anticorps (AA 1-265) (ABIN1885866)

Antigène: PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX26 est non-conjugé

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

Détail du produit anti-PEX26 anticorps

Épitope: AA 1-265

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 265 of Human PEX26

Information d'application

Indications d'application: Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.50-1.500
Immunofluorescence: 1.100-1.200

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: Biohazard Informations: This product contains thimerosal which is hazardous.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.

Détails sur PEX26

Antigène: PEX26 (Peroxisomal Biogenesis Factor 26 (PEX26))

Autre désignation: Peroxin 26

Sujet: This gene belongs to the peroxin-26 gene family.It is probably required for protein import into peroxisomes.It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes.Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8).PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix.The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP).Two transcript variants encoding the same protein have been identified for this gene.[provided by RefSeq]

Poids moléculaire: 34 kDa

ID gène: 55670

NCBI Accession: NP_060399, NM_017929