PEX1 anticorps (AA 599-628)

N° du produit ABIN5538265

Détail du produit anti-PEX1 anticorps

Antigène: PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

Épitope: AA 599-628

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX1 est non-conjugé

Application: Western Blotting (WB)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This PEX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 599-628 amino acids from the Central region of human PEX1.

Isotype: Ig Fraction

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

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.

Stock: 4 °C,-20 °C

Stockage commentaire: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Détails sur PEX1

Antigène: PEX1 (Peroxisomal Biogenesis Factor 1 (PEX1))

Autre désignation: PEX1 (PEX1 Produits)

Synonymes: anticorps PBD1A, anticorps PBD1B, anticorps ZWS, anticorps ZWS1, anticorps 5430414H02Rik, anticorps E330005K07Rik, anticorps RGD1559939, anticorps pex1, anticorps peroxisomal biogenesis factor 1, anticorps peroxisomal biogenesis factor 1 L homeolog, anticorps PEX1, anticorps Pex1, anticorps pex1.L

Sujet: This gene encodes a member of the AAA ATPase family, a large group of ATPases associated with diverse cellular activities. This protein is cytoplasmic but is often anchored to a peroxisomal membrane where it forms a heteromeric complex and plays a role in the import of proteins into peroxisomes and peroxisome biogenesis. Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome.

Poids moléculaire: 143 kDa

ID gène: 5189

UniProt: O43933