Phenylalanine Hydroxylase anticorps (AA 71-208) (Fluoro594)

N° du produit ABIN8021069

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

Aperçu rapide pour Phenylalanine Hydroxylase anticorps (AA 71-208) (Fluoro594) (ABIN8021069)

Antigène: Phenylalanine Hydroxylase

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Phenylalanine Hydroxylase est conjugé à/à la Fluoro594

Application: Flow Cytometry (FACS)

Détail du produit anti-Phenylalanine Hydroxylase anticorps (Fluoro594)

Épitope: AA 71-208

Fonction: Anti-PAH Antibody Fluoro594 Conjugated

Specificité: No cross reactivity with other proteins.

Réactivité croisée (Details): No cross-reactivity with other proteins.

Homologie: coli-derived human PAH recombinant protein (Position: R71-H208). Human PAH shares 89.1%,88.4% amino acid (aa) sequence identity with mouse,rat PAH,respectively.

Purification: Immunogen affinity purified.

Immunogène: E. coli-derived human PAH recombinant protein (Position: R71-H208). Human PAH shares 89.1% and 88.4% amino acid (aa) sequence identity with mouse and rat PAH, respectively.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur Phenylalanine Hydroxylase

Antigène: Phenylalanine Hydroxylase

Autre désignation: PAH

Sujet:

Background: Phenylalanine hydroxylase (PAH) is an enzyme that catalyzes the hydroxylation of the aromatic side-chain of phenylalanine to generate tyrosine. It is one of three members of the biopterin-dependent aromatic amino acid hydroxylases, a class of monooxygenase that uses tetrahydrobiopterin (BH4, a pteridine cofactor) and a non-heme iron for catalysis. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria.

Gene Full Name: phenylalanine hydroxylase

ID gène: 5053

UniProt: P00439