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Rabbit anti-Human TIAL1 Polyclonal Antibody

The antibody against TIAL1 was raised in rabbit using the Recombinant Human Nucleolysin TIAR protein (9-277AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IF.

ADC-00937A

The antibody against TIAL1 was raised in rabbit using the Recombinant Human Nucleolysin TIAR protein (9-277AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IF.

$299.00

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Specifications


Cat.No ADC-00937A ClonalityPolyclonal
Host SpeciesRabbitTarget NameTIAL1
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IFStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Nucleolysin TIAR protein (9-277AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ01085
Background Information
  • Uniprot Id

    Q01085

  • Target Species

    Human

  • Target Name

    TIAL1

  • Target Full Name

    Nucleolysin TIAR

  • Target Function

    RNA-binding protein. Possesses nucleolytic activity against cytotoxic lymphocyte target cells. May be involved in apoptosis.

  • Target Subcellular Location

    Cytoplasm. Nucleus. Cytolytic granule. Cytoplasm, Stress granule.

  • Target Synonyms

    TCBP; TIAR; TIAL1

  • Target Background

    The protein encoded by this gene is a member of a family of RNA-binding proteins, has three RNA recognition motifs (RRMs), and binds adenine and uridine-rich elements in mRNA and pre-mRNAs of a wide range of genes. It regulates various activities including translational control, splicing and apoptosis. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. The different isoforms have been show to function differently with respect to post-transcriptional silencing.

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