Phenylalanine Hydroxylase anticorps (AA 132-161)

N° du produit ABIN651111

Détail du produit anti-Phenylalanine Hydroxylase anticorps

Antigène: Phenylalanine Hydroxylase

Épitope: AA 132-161

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Phenylalanine Hydroxylase est non-conjugé

Application: Western Blotting (WB)

Homologie: B, Rat

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This PAH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 132-161 amino acids from the Central region of human PAH.

Clone: RB24519

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur Phenylalanine Hydroxylase

Antigène: Phenylalanine Hydroxylase

Autre désignation: PAH (Phenylalanine Hydroxylase Produits)

Synonymes: anticorps cb877, anticorps wu:fb02f10, anticorps zgc:65981, anticorps GB18494, anticorps PAH, anticorps pku, anticorps pku1, anticorps DDBDRAFT_0206188, anticorps DDBDRAFT_0231664, anticorps DDB_0206188, anticorps DDB_0231664, anticorps AW106920, anticorps PH, anticorps PKU, anticorps PKU1, anticorps phenylalanine-4-hydroxylase, anticorps phenylalanine hydroxylase, anticorps protein henna, anticorps phenylalanine 4-monooxygenase, anticorps pah, anticorps LOC408622, anticorps PAH, anticorps CpipJ_CPIJ002149, anticorps Pah

Classe de substances: Chemical

Sujet: PAH 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: 51862

ID gène: 5053

NCBI Accession: NP_000268

UniProt: P00439