|Other Names||Fumarylacetoacetase, FAA, Beta-diketonase, Fumarylacetoacetate hydrolase, FAH|
|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.|
|Tissue Location||Mainly expressed in liver and kidney. Lower levels are also detected in many other tissues|
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Provided below are standard protocols that you may find useful for product applications.
This gene encodes the last enzyme in the tyrosinecatabolism pathway. FAH deficiency is associated with Type 1hereditary tyrosinemia (HT).
Joslyn, G., et al. Alcohol. Clin. Exp. Res. 34(5):800-812(2010)Liu, J., et al. Hum Brain Mapp 30(1):241-255(2009)Ferreira, M.A., et al. Nat. Genet. 40(9):1056-1058(2008)Bliksrud, Y.T., et al. J. Mol. Med. 83(5):406-410(2005)Dreumont, N., et al. BMC Mol. Biol. 6 (1), 1 (2005) :
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