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Rabbit anti-Human HAL Polyclonal Antibody, HRP conjugated

The antibody against HAL was raised in rabbit using the Recombinant Human Histidine ammonia-lyase protein (36-152AA) as the immunogen. This antibody exists as a hrp conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA.

ADC-06034A

The antibody against HAL was raised in rabbit using the Recombinant Human Histidine ammonia-lyase protein (36-152AA) as the immunogen. This antibody exists as a hrp conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA.

$299.00

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Specifications


Cat.No ADC-06034A ClonalityPolyclonal
Host SpeciesRabbitTarget NameHAL
Target Synonymsdy; hutH 1 antibody; Hal antibody; HAL protein antibody; Histidase antibody; Histidine ammonia lyase antibody; Histidine ammonia-lyase antibody; HSTD antibody; HutH antibody; HUTH_HUMAN antibodyFormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4Purification Method>95%, Protein G purified
ConjugateHRP conjugatedApplicationELISA
StorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Histidine ammonia-lyase protein (36-152AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP42357
Background Information
  • Uniprot Id

    P42357

  • Target Species

    Human

  • Target Name

    HAL

  • Target Full Name

    Histidine ammonia-lyase

  • Target Involvement

    Histidinemia (HISTID)

  • Target Protein Families

    PAL/histidase family

  • Target Synonyms

    IS; hutH 1; Hal; HAL protein; Histidase; Histidine ammonia lyase; Histidine ammonia-lyase; HSTD; HutH; HUTH_HUMAN

  • Target Background

    Histidine ammonia-lyase is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. Histidine ammonia-lyase defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluids. Several transcript variants encoding different isoforms have been found for this gene.

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