Phenylalanine Hydroxylase anticorps

N° du produit ABIN7467130

L’anticorps Lapin Polyclonal anti-Phenylalanine Hydroxylase a été validé pour WB, ICC et IF. Il convient pour détecter Phenylalanine Hydroxylase dans des échantillons de Humain.

Aperçu rapide pour Phenylalanine Hydroxylase anticorps (ABIN7467130)

Antigène: Phenylalanine Hydroxylase

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Phenylalanine Hydroxylase est non-conjugé

Application: Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)

Détail du produit anti-Phenylalanine Hydroxylase anticorps

Réactivité croisée: Humain

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human PAH. 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:

Validation: Orthogonal

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1.76 mg/mL

Buffer: 1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: 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 Phenylalanine Hydroxylase

Antigène: Phenylalanine Hydroxylase

Sujet: Phenylalanine hydroxylase , PH , PKU , PKU1,This gene encodes a member of the biopterin-dependent aromatic amino acid hydroxylase protein family. The encoded phenylalanine hydroxylase enzyme hydroxylates phenylalanine to tyrosine and is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria. [provided by RefSeq, Aug 2017]

Poids moléculaire: 52 kDa

ID gène: 5053

UniProt: P00439