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

N° du produit ABIN8021071

Cet anticorps anti-Phenylalanine Hydroxylase Polyclonal Lapin conjugué à HRP (ABIN8021071) détecte spécifiquement Phenylalanine Hydroxylase dans WB, IHC et ELISA. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour Phenylalanine Hydroxylase anticorps (AA 71-208) (HRP) (ABIN8021071)

Antigène: Phenylalanine Hydroxylase

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

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

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

Détail du produit anti-Phenylalanine Hydroxylase anticorps (HRP)

Épitope: AA 71-208

Fonction: Anti-PAH Antibody HRP 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: Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, 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.

Stock: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

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