FAH Polyclonal Antibody | G-AB-06379

FAH Polyclonal Antibody | G-AB-06379 | Gentaur Antibodies

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

Category Type: Polyclonal Antibody

Research Areas: Metabolism, Signal Transduction

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

Reactivity: Human, Mouse, Rat

Host: Rabbit

Isotype: IgG

Gene ID:

Accession #: BC002527

Clonality: Polyclonal

Immunogen: Fusion protein of human FAH

Clone #:

Conjugation: Unconjugated

Swissprot: P16930

Santa Cruz:

Calculated MW: 46 kDa

Observed MW: Refer to figures

Concentration: 1.3 mg/mL

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

Purification method: Antigen affinity purification

Application: WB, IHC, ELISA

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.

FAH Polyclonal Antibody DataSheet