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Rabbit anti-Human RSPH14 Polyclonal Antibody

The antibody against RSPH14 was raised in rabbit using the Recombinant Human Radial spoke head 14 homolog protein (1-230AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, WB, IHC.

ADC-23744A

The antibody against RSPH14 was raised in rabbit using the Recombinant Human Radial spoke head 14 homolog protein (1-230AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, WB, IHC.

$299.00

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Specifications


Cat.No ADC-23744A ClonalityPolyclonal
Host SpeciesRabbitTarget NameRSPH14
Target Synonyms4933431K05Rik antibody; MCG5994, isoform CRA_b antibody; MGC16968 antibody; Rhabdoid tumor deletion region gene 1 antibody; Rhabdoid tumor deletion region protein 1 antibody; RTDR1 antibody; RTDR1_HUMAN antibodyFormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4Purification Method>95%, Protein G purified
ConjugateNon-conjugatedApplicationELISA, IHC, WB
StorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Radial spoke head 14 homolog protein (1-230AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ9UHP6
Background Information
  • Uniprot Id

    Q9UHP6

  • Target Species

    Human

  • Target Name

    RSPH14

  • Target Full Name

    Radial spoke head 14 homolog

  • Target Synonyms

    4933431K05Rik; MCG5994, isoform CRA_b; MGC16968; Rhabdoid tumor deletion region gene 1; Rhabdoid tumor deletion region protein 1; RTDR1; RTDR1_HUMAN

  • Target Background

    This gene encodes a protein with no known function but with slight similarity to a yeast vacuolar protein. The gene is located in a region deleted in pediatric rhabdoid tumors of the brain, kidney and soft tissues, but mutations in this gene have not been associated with the disease.

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