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Rabbit anti-Human FAH Monoclonal Antibody

The antibody against FAH was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-419 of human FAH (NP_000128.1) as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, IF/ICC, ELISA.

ADA-15748A

The antibody against FAH was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-419 of human FAH (NP_000128.1) as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IHC-P, IF/ICC, ELISA.

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Specifications


Cat.No ADA-15748A ClonalityMonoclonal
Host SpeciesRabbitTarget NameFAH
FormLiquidSpecies ReactivityHuman, Mouse, Rat
IsotypeIgGStorage Buffer50% Glycerol, 0.05% BSA, PBS with 0.05% proclin300, pH7.3.
Purification MethodAffinity purificationPositive SamplesMouse kidney
ApplicationELISA, WB, IF/ICC, IHC-P

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 1-419 of human FAH (NP_000128.1).Target SpeciesHuman
Uniprot IDP16930Immunogen Sequence
Background Information
  • Uniprot Id

    P16930

  • Target Species

    Human

  • Target Name

    FAH

  • Target Full Name

    Fumarylacetoacetase

  • Target Involvement

    Tyrosinemia 1 (TYRSN1)

  • Target Protein Families

    FAH family

  • Target Tissue Specificity

    Mainly expressed in liver and kidney. Lower levels are also detected in many other tissues.

  • Target Synonyms

    FAHFumarylacetoacetase; FAA; EC 3.7.1.2; Beta-diketonase; Fumarylacetoacetate hydrolase

  • Target Background

    Predicted to enable fumarylacetoacetase activity. Predicted to be involved in L-phenylalanine catabolic process; homogentisate catabolic process; and tyrosine catabolic process. Predicted to act upstream of or within arginine catabolic process. Located in extracellular exosome. Implicated in tyrosinemia type I.

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