FAH antibody - C-terminal region

Cat# ARP41681_T100

Size : 100ul

Brand : Aviva Systems Biology

Request more information

Contact local distributor :


Phone : +1 850 650 7790

FAH Antibody - C-terminal region (ARP41681_T100)

Datasheets/ManualsPrintable datasheet for anti-FAH (ARP41681_T100) antibody
Product Info
Publications

Functional and Biochemical Characterization of Hepatitis C Virus (HCV) Particles Produced in a Humanized Liver Mouse Model. J. Biol. Chem. 290, 23173-87 (2015). 2622463324465277

More...

Tested Species ReactivityHuman, Mouse
Predicted Species ReactivityHuman, Mouse, Rat, Cow, Dog, Guinea Pig, Horse, Rabbit, Zebrafish
Product FormatLiquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
ClonalityPolyclonal
HostRabbit
ApplicationIHC, WB
Additional InformationIHC Information: Human Liver: Formalin-Fixed, Paraffin-Embedded (FFPE)
IHC Information: Human Liver: Formalin-Fixed, Paraffin-Embedded (FFPE)
Reconstitution and StorageFor short term use, store at 2-8C up to 1 week. For long term storage, store at -20C in small aliquots to prevent freeze-thaw cycles.
ImmunogenThe immunogen is a synthetic peptide directed towards the C terminal region of human FAH
PurificationProtein A purified
Predicted Homology Based on Immunogen SequenceCow: 93%; Dog: 100%; Guinea Pig: 93%; Horse: 100%; Human: 100%; Mouse: 100%; Rabbit: 93%; Rat: 100%; Zebrafish: 93%
Peptide SequenceSynthetic peptide located within the following region: AATICKSNFKYMYWTMLQQLTHHSVNGCNLRPGDLLASGTISGPEPENFG
Concentration1.0 mg/ml
Blocking PeptideFor anti-FAH (ARP41681_T100) antibody is Catalog # AAP41681 (Previous Catalog # AAPP24324)
Other Applications Image 1 DataSample Type: Human Liver and Mouse FAH KO liver
Primary Dilution: 1:400
ReferenceBliksrud,Y.T., (2005) J. Mol. Med. 83 (5), 406-410
Gene SymbolFAH
Gene Full NameFumarylacetoacetate hydrolase (fumarylacetoacetase)
NCBI Gene Id2184
Protein NameFumarylacetoacetase
Description of TargetFAH is the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia.This gene encodes the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia (HT).
Uniprot IDP16930
Protein Accession #NP_000128
Nucleotide Accession #NM_000137
Protein Size (# AA)419
Molecular Weight46kDa
Protein InteractionsKRTAP10-8; ADAMTSL4; SERTAD1; TCF4; KRTAP5-9; UBC; EGFR;