Fumarylacetoacetate Hydrolase (FAH) Antibody

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Catalogue No: abx026534
Price: US$326.25
(Size: 80 µl)

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Documents

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

Target Fumarylacetoacetate Hydrolase (FAH)
Clonality Polyclonal
Reactivity Human
Tested Applications ELISA, WB, IHC, IF/ICC
Host Rabbit
Recommended dilutions WB: 1/1000, IHC-P: 1/50 - 1/100, IF/ICC: 1/10 - 1/50. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user.
Conjugation Unconjugated
Immunogen KLH-conjugated synthetic peptide between 7-33 amino acids from the N-terminal region of human FAH.
Isotype IgG
Form Liquid
Purification Purified through a protein A column, followed by peptide affinity purification.
Storage Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
UniProt Primary AC P16930 (UniProt, ExPASy)
UniProt Secondary AC B2R9X1, D3DW95, Q53XA7
UniProt Entry Name FAAA_HUMAN
Gene Symbol FAH
KEGG hsa:2184
String 9606.ENSP00000385080
Molecular Weight Calculated MW: 46.4 kDa
Buffer PBS containing 0.09% sodium azide.
Availability Shipped within 5-10 working days.
Note THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.
Research Articles on Fumarylacetoacetate Hydrolase (FAH)


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