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IVD Test Reagent/Kits, Molecular Assay, Gene Anomaly, Mutation, PAH

Definition : Molecular assay reagents intended to identify mutations in the phenylalanine hydroxylase (PAH) gene, located at chromosome 12q22-q24.2, which encodes for the enzyme phenylalanine hydroxylase. The enzyme is responsible for the first step in processing phenylalanine, an amino acid obtained through the diet. Mutations at this locus have been identified in patients with phenylketonuria (PKU).

Entry Terms : "Variant Phenylketonuria Gene Mutation Reagents" , "Hyperphenylalaninemia (HPA) Gene Mutation Reagents" , "Phenylketonuria (PKU) Gene Mutation Reagents" , "Phenylalanine Hydroxylase (PAH) Deficiency Gene Mutation Reagents" , "PAH Gene Mutation Detection Reagents" , "Reagents, Molecular Assay, Gene Anomaly, Mutation, PAH"

UMDC code : 24650

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Brand-Nu Laboratories Inc

Company Type: Parent

Mayo Medical Laboratories

Company Type: Parent

PerkinElmer Inc

Company Type: Parent

As a global technology leader, PerkinElmer is taking action to harness the power of insights and transform them into knowledge to deliver innovative, differentiated solutions for our customers. From critical therapeutic and disease research and prenatal screening, to environmental testing and industrial monitoring, we are actively engaged in improving health and advancing quality and longevity of life all around the world.

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