FAH Polyclonal Antibody

Background:
This gene encodes the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia (HT).

Research Area: Metabolism, Signal transduction

Synonyms:
Beta diketonase, FAA, FAH, Fumarylacetoacetase, Fumarylacetoacetate, Fumarylacetoacetate hydrolase

Immunogen: Fusion protein of human FAH

Swissprot: P16930
Gene Accession: BC002527

Calculated MW: 46 kDa
Observed MW: Refer to figures

Purification Method: Antigen affinity purification

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Concentration: 1.3 mg/mL
Dilution: WB 1:500-1:2000, IHC 1:50-1:300, ELISA 1:5000-1:10000

Storage:
Store at -20°C. Avoid freeze / thaw cycles.