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Rabbit anti-Human SMS Polyclonal Antibody

The antibody against SMS was raised in rabbit using the Recombinant Human Spermine synthase protein (16-191AA) 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, IHC, IF.

ADC-14537A

The antibody against SMS was raised in rabbit using the Recombinant Human Spermine synthase protein (16-191AA) 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, IHC, IF.

$299.00

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Specifications


Cat.No ADC-14537A ClonalityPolyclonal
Host SpeciesRabbitTarget NameSMS
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4
Purification Method>95%, Protein G purifiedConjugateNon-conjugated
ApplicationELISA, IF, IHCStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Spermine synthase protein (16-191AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP52788
Background Information
  • Uniprot Id

    P52788

  • Target Species

    Human

  • Target Name

    SMS

  • Target Full Name

    Spermine synthase

  • Target Function

    Catalyzes the production of spermine from spermidine and decarboxylated S-adenosylmethionine (dcSAM).

  • Target Involvement

    X-linked syndromic mental retardation Snyder-Robinson type (MRXSSR)

  • Target Protein Families

    Spermidine/spermine synthase family

  • Target Synonyms

    MRSR; SMS; Snyder Robinson X linked mental retardation syndrome; Spermidine aminopropyltransferase; Spermine synthase; SPMSY; SpS; SPSY_HUMAN; SRS

  • Target Background

    This gene encodes a protein belonging to the spermidine/spermin synthase family and catalyzes the production of spermine from spermidine. Pseudogenes of this gene are located on chromosomes 1, 5, 6 and X. Mutations in this gene cause an X-linked intellectual disability called Snyder-Robinson Syndrome (SRS). Multiple transcript variants encoding different isoforms have been found for this gene.

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