Anti-FAH Polyclonal Antibody, 100.0ul
£243.06
Delivery: 2 weeks
SKU
K106957P-100.0ul
This gene encodes the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia (HT).
This gene encodes the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia (HT).
- Size: 100.0ul
- Molecular Weight: 46kDa
- Physical State: Liquid
- Storage: Store at -20℃. Avoid freeze/thaw cycles.
- Application: IHC;WB
- Brand: Saint Michael
- Catalogue No.: K106957P-100.0ul
For laboratory research use only. Not for human or animal consumption, diagnostic or therapeutic use.
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