PEX6 anticorps

N° du produit ABIN2854607

L’anticorps Lapin Polyclonal anti-PEX6 a été validé pour WB. Il convient pour détecter PEX6 dans des échantillons de Humain.

Aperçu rapide pour PEX6 anticorps (ABIN2854607)

Antigène: PEX6 (Peroxisomal Biogenesis Factor 6 (PEX6))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX6 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-PEX6 anticorps

Réactivité croisée: Humain

Attributs du produit: Rabbit polyclonal antibody to PEX6 (peroxisomal biogenesis factor 6)
PEX6 antibody

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human PEX6. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: A549

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur PEX6

Antigène: PEX6 (Peroxisomal Biogenesis Factor 6 (PEX6))

Autre désignation: peroxisomal biogenesis factor 6

Sujet: This gene encodes a member of the AAA (ATPases associated with diverse cellular activities) family of ATPases. This member is a predominantly cytoplasmic protein, which plays a direct role in peroxisomal protein import and is required for PTS1 (peroxisomal targeting signal 1, a C-terminal tripeptide of the sequence ser-lys-leu) receptor activity. Mutations in this gene cause peroxisome biogenesis disorders of complementation group 4 and complementation group 6.

Cellular Localization: Cytoplasm , Peroxisome membrane

Poids moléculaire: 104 kDa

ID gène: 5190

UniProt: Q13608