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FAH antibody (N-Term)
This Rabbit Polyclonal antibody specifically detects FAH in WB, IF and IHC (p). It exhibits reactivity toward Human.
Catalog No. ABIN655906
$383.35
$451.00
save $67.65 (-15 %)
Plus shipping costs $50.00
80 μL ABIN2845306
400 μL ABIN655906
80 μL ABIN2845306
400 μL ABIN655906
Delivery in 10 to 11 Business Days
Quick Overview for FAH antibody (N-Term) (ABIN655906)
Target
See all FAH Antibodies
FAH
(Fumarylacetoacetate Hydrolase (Fumarylacetoacetase) (FAH))
Reactivity
All reactivities for FAH antibodies
Human
Host
All hosts for FAH antibodies
Rabbit
Clonality
All clonalities for FAH antibodies
Polyclonal
Conjugate
All conjugates for FAH antibodies
This FAH antibody is un-conjugated
Application
All applications for FAH antibodies
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
Clone
RB19635
Product Details anti-FAH Antibody
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Binding Specificity
All epitopes for FAH antibodies
AA 7-33, N-Term
Purification
This antibody is purified through a protein A column, followed by peptide affinity purification.
Immunogen
This FAH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 7-33 amino acids from the N-terminal region of human FAH.
Isotype
Ig Fraction
Alternatives
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Application Details
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Application Notes
IF: 1:10~50. WB: 1:1000. IHC-P: 1:50~100
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
4 °C,-20 °C
Storage Comment
Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
Expiry Date
6 months
Target Details for FAH
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Target
FAH
(Fumarylacetoacetate Hydrolase (Fumarylacetoacetase) (FAH))
Alternative Name
FAH
Background
This gene encodes the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia (HT).
Molecular Weight
46374
Gene ID
2184
NCBI Accession
NP_000128
UniProt
P16930
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