Learn More
Description
This gene encodes the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia (HT). [provided by RefSeq
Specifications
Specifications
| Antigen | FAH |
| Applications | ELISA, Immunohistochemistry (PFA fixed), Western Blot |
| Classification | Monoclonal |
| Clone | 665a3 |
| Concentration | 1 ug/uL |
| Conjugate | Unconjugated |
| Description | Mouse monoclonal antibody raised against full length recombinant FAH. |
| Dilution | Western Blot (1:1000) The optimal working dilution should be determined by the end user. |
| Formulation | In citrate-Tris-HCl, pH 7.0 (0.02% Proclin 300) |
| Gene | FAH |
| Show More |
By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.