Cat: IPD-X28622

Recombinant Human SLC34A3 Protein (HEK293),Flag & Strep

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Analytical Data

  • Gene name

    SLC34A3

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    NPT2C; NPTIIC

  • Species

    Human

  • Source

    HEK293

  • Tag

    Strep;His;Flag

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q8N130

  • Expression Region

    P2-L598

  • Protein Length

    Partial

  • Endotoxin

    < 1.0 EU per μg protein as determined by the LAL method.

  • Form

    Freeze-dried powder

  • Buffer formulation

    PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.

  • Reconstitution

    Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.

  • Customization

    Site-directed mutagenesis Custom tag design Custom buffer formulation Custom full-length protein production

  • Stability Test

    The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.

  • Storage & Shelf Life

    Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.

  • Shipping

    In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.

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Protein Description

SLC34A3, a member of the SLC34 family of sodium-dependent phosphate transporters, plays a crucial role in maintaining phosphate homeostasis in the body. This protein is primarily expressed in the kidneys and intestines, where it facilitates the reabsorption of phosphate from the renal tubules and absorption from the gastrointestinal tract. Mutations in the SLC34A3 gene can lead to familial hypophosphatemic rickets, a disorder characterized by impaired phosphate reabsorption resulting in phosphate wasting, bone pain, and growth abnormalities in children. Given the significance of phosphate in various biological processes, including energy metabolism, skeletal health, and cellular signaling, understanding the functional properties of SLC34A3 is essential. Recombinant SLC34A3 protein studies provide valuable insights into its transport mechanism, substrate specificity, and regulatory pathways. Furthermore, by analyzing its interactions with other cellular proteins and assessing its pharmacological properties, researchers aim to uncover potential therapeutic targets for conditions associated with phosphate dysregulation. The recombinant expression and purification of SLC34A3 not only facilitate structural and functional analyses but also contribute to the development of novel strategies to ameliorate diseases resulting from SLC34A3 dysfunction. This research area is increasingly important as it intersects with broader implications related to bone health, mineral metabolism, and the development of treatment modalities for metabolic disorders.

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