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Rabbit anti-Human SLC52A3 Polyclonal Antibody

The antibody against SLC52A3 was raised in rabbit using the Recombinant Human Solute carrier family 52, riboflavin transporter, member 3 protein (159-220AA) 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, IF.

ADC-14179A

The antibody against SLC52A3 was raised in rabbit using the Recombinant Human Solute carrier family 52, riboflavin transporter, member 3 protein (159-220AA) 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, IF.

$299.00

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Specifications


Cat.No ADC-14179A ClonalityPolyclonal
Host SpeciesRabbitTarget NameSLC52A3
Target Synonymsmember 3 antibody, member 3 antibody; S52A3_HUMAN antibody; Slc52a3 antibody; solute carrier family 52 (riboflavin transporter), member 3 antibody; Solute carrier family 52 antibody; solute carrier family 52, riboflavin transporterFormLiquid
Species ReactivityHuman, MouseIsotypeIgG
Storage Buffer0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4Purification Method>95%, Protein G purified
ConjugateNon-conjugatedApplicationELISA, IF, IHC, WB
StorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Solute carrier family 52, riboflavin transporter, member 3 protein (159-220AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ9NQ40
Background Information
  • Uniprot Id

    Q9NQ40

  • Target Species

    Human

  • Target Name

    SLC52A3

  • Target Full Name

    Solute carrier family 52, riboflavin transporter, member 3

  • Target Function

    Plasma membrane transporter mediating the uptake by cells of the water soluble vitamin B2/riboflavin that plays a key role in biochemical oxidation-reduction reactions of the carbohydrate, lipid, and amino acid metabolism. Humans are unable to synthesize vitamin B2/riboflavin and must obtain it via intestinal absorption.

  • Target Involvement

    Brown-Vialetto-Van Laere syndrome 1 (BVVLS1); Fazio-Londe disease (FALOND)

  • Target Subcellular Location

    Apical cell membrane; Multi-pass membrane protein. Cell membrane.; [Isoform 1]: Cell membrane; Multi-pass membrane protein. Nucleus membrane; Multi-pass membrane protein. Cytoplasm.; [Isoform 2]: Cytoplasm.

  • Target Protein Families

    Riboflavin transporter family

  • Target Tissue Specificity

    Predominantly expressed in testis. Highly expressed in small intestine and prostate.

  • Target Synonyms

    bA371L19.1; BVVLS; BVVLS1; C20orf54; C20orf54provided by HGNC; Chromosome 20 open reading frame 54; hRFT2; member 3; MGC10698; RFT2; RFVT3; Riboflavin transporter 2; riboflavin transporter; riboflavin transporter, member 3; S52A3_HUMAN; Slc52a3; solute carrier family 52 (riboflavin transporter), member 3; Solute carrier family 52; solute carrier family 52, riboflavin transporter, member 3

  • Target Background

    This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin. The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus. Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease.

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