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PAH (R400) Peptide

PAH (R400) Peptide

Cat no: BS3704P

Supplier: Bioworld Technology, Inc.
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The PAH gene encodes the enzyme phenylalanine hydroxylase (PAH), which converts phenylalanine to tyrosine and is the rate-limiting enzyme in phenylalanine catabolism. Mammalian PAH is a soluble, homotetrameric protein which is abundantly expressed in human liver. Deficiency of PAH activity results in the autosomal recessive disorder phenylketonuria (PKU), which is characterized by mental retardation unless a low phenylalanine diet is introduced early in life. The PAH gene, which maps to human chromosome 12q23.2, contains all the genetic information necessary to code for functional PAH, demonstrating that a single gene is involved in the classic disease phenotype.
Catalogue number: BS3704P
Applications: Block/Neutralize/Inhibit
Swiss prot: P00439
Form: 1 mg/ml in DI water.
Purity: Synthetic peptide PAH (R400). (Note: the amino acid sequence is proprietary). The purity is > 98%.
Storage temp: Store at 4 degree C short term. Aliquot and store at -20 degree C long term. Avoid freeze-thaw cycles.
Alternative names: Phenylalanine-4-hydroxylase; PAH; Phe-4-monooxygenase
Additional info: This peptide can be used with studies using BS3704 PAH (R400) pAb.

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