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:
FAH

Immunogen: Recombinant fusion protein of human FAH (NP_000128.1).

Swissprot: P16930
Gene ID: 2184

Calculated MW: 38 kDa/46 kDa
Observed MW: 46 kDa

Purification Method: Affinity purification

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Concentration: 1 mg/mL
Dilution: "WB 1:500-1:2000 IHC 1:50-1:200"

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