Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Store as concentrated solution.
Centrifuge briefly prior to opening vial.
This gene encodes the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia (HT).
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Beta-diketonase; FAA; Fumarylacetoacetase; Fumarylacetoacetate hydrolase; fumarylacetoacetate hydrolase (fumarylacetoacetase)
Gene Aliases: FAH
UniProt ID: (Human) P16930, (Rat) P25093, (Mouse) P35505
Entrez Gene ID: (Human) 2184, (Rat) 29383, (Mouse) 14085
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