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FAH Antibody (N-term) Blocking peptide
Synthetic peptide
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
| Primary Accession | P16930 |
|---|---|
| Clone Names | 81006139 |
| Gene ID | 2184 |
|---|---|
| Other Names | Fumarylacetoacetase, FAA, Beta-diketonase, Fumarylacetoacetate hydrolase, FAH |
| Format | Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed. |
| Storage | Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C. |
| Precautions | This product is for research use only. Not for use in diagnostic or therapeutic procedures. |
| Name | FAH |
|---|---|
| Tissue Location | Mainly expressed in liver and kidney. Lower levels are also detected in many other tissues |
Thousands of laboratories across the world have published research that depended on the performance of antibodies from Abcepta to advance their research. Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.
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Provided below are standard protocols that you may find useful for product applications.
Background
This gene encodes the last enzyme in the tyrosinecatabolism pathway. FAH deficiency is associated with Type 1hereditary tyrosinemia (HT).
References
Joslyn, G., et al. Alcohol. Clin. Exp. Res. 34(5):800-812(2010)Liu, J., et al. Hum Brain Mapp 30(1):241-255(2009)Ferreira, M.A., et al. Nat. Genet. 40(9):1056-1058(2008)Bliksrud, Y.T., et al. J. Mol. Med. 83(5):406-410(2005)Dreumont, N., et al. BMC Mol. Biol. 6 (1), 1 (2005) :
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