|Other Names||Phenylalanine-4-hydroxylase, PAH, Phe-4-monooxygenase, PAH|
|Format||Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.|
|Storage||Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.|
|Precautions||This product is for research use only. Not for use in diagnostic or therapeutic procedures.|
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Provided below are standard protocols that you may find useful for product applications.
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.
Bonyadi, M., et al. Genet Test Mol Biomarkers 14(2):233-235(2010)Dupuis, J., et al. Nat. Genet. 42(2):105-116(2010)Santos, L.L., et al. Genet. Mol. Res. 9(1):1-8(2010)
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