PEX13 anticorps (C-Term)

N° du produit ABIN2856329

L’anticorps Lapin Polyclonal anti-PEX13 a été validé pour WB et IHC (p). Il convient pour détecter PEX13 dans des échantillons de Humain.

Aperçu rapide pour PEX13 anticorps (C-Term) (ABIN2856329)

Antigène: PEX13 (Peroxisomal Biogenesis Factor 13 (PEX13))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp PEX13 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-PEX13 anticorps

Épitope: C-Term

Réactivité croisée: Humain

Attributs du produit: Rabbit polyclonal antibody to PEX13 (peroxisome biogenesis factor 13)
PEX13 antibody [C3], C-term

Purification: Purified by antigen-affinity chromatography.

Immunogène: Carrier-protein conjugated synthetic peptide encompassing a sequence within the C-terminus region of human PEX13. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: Molt-4

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( 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 PEX13

Antigène: PEX13 (Peroxisomal Biogenesis Factor 13 (PEX13))

Autre désignation: peroxisomal biogenesis factor 13

Sujet: This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm. Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome.

Cellular Localization: Peroxisome membrane, Single-pass membrane protein

Poids moléculaire: 44 kDa

ID gène: 5194

UniProt: Q92968

Pathways: Feeding Behaviour, Monocarboxylic Acid Catabolic Process