Phenylalanine Hydroxylase anticorps (C-Term)

N° du produit ABIN7216436

Cet anticorps Lapin Polyclonal détecte spécifiquement Phenylalanine Hydroxylase dans WB, IHC, ELISA et IF. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour Phenylalanine Hydroxylase anticorps (C-Term) (ABIN7216436)

Antigène: Phenylalanine Hydroxylase

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Phenylalanine Hydroxylase est non-conjugé

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

Détail du produit anti-Phenylalanine Hydroxylase anticorps

Épitope: C-Term

Fonction: Rabbit Anti-PAH Polyclonal Antibody

Specificité: PAH Polyclonal Antibody detects endogenous levels of PAH protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from the C-terminal region of human PAH

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000,IHC 1:100-1:300,ELISA 1:40000,IF 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % 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: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur Phenylalanine Hydroxylase

Antigène: Phenylalanine Hydroxylase

Autre désignation: PAH

Sujet: PAH, Phenylalanine-4-hydroxylase, PAH, Phe-4-monooxygenasePAH encodes the enzyme phenylalanine hydroxylase that is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria.

Poids moléculaire: 51kD

ID gène: 5053

UniProt: P00439