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Recombinant Human Sodium/iodide cotransporter (SLC5A5), Truncated

ACP05933

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP05933 Target NameSLC5A5
Target Synonymsmember 5; Solute carrier family 5 member 5; TDH1FormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Protein LengthPartial
Purity>85% (SDS-PAGE)Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDQ92911
Background Information
  • Uniprot Id

    Q92911

  • Target Species

    Human

  • Target Name

    SLC5A5

  • Target Full Name

    Sodium/iodide cotransporter

  • Target Function

    Mediates iodide uptake in the thyroid gland.

  • Target Involvement

    Thyroid dyshormonogenesis 1 (TDH1)

  • Target Subcellular Location

    Membrane; Multi-pass membrane protein.

  • Target Protein Families

    Sodium:solute symporter (SSF) (TC 2.A.21) family

  • Target Tissue Specificity

    Expression is primarily in thyroid tissue, but also to a lower extent in mammary gland and ovary. Expression is reduced in tumors.

  • Target Research Area

    Others

  • Target Synonyms

    Na(+)/I(-) cotransporter; Na(+)/I(-) symporter; Na+/I- cotransporter; Na+/I-symporter; NIS; SC5A5_HUMAN; Slc5a5; sodium iodide symporter; Sodium-iodide symporter; Sodium/iodide cotransporter; Solute carrier family 5 (sodium iodide symporter) member 5; solute carrier family 5 (sodium/iodide cotransporter), member 5; Solute carrier family 5 member 5; TDH1

  • Target Background

    This gene encodes a member of the sodium glucose cotransporter family. The encoded protein is responsible for the uptake of iodine in tissues such as the thyroid and lactating breast tissue. The iodine taken up by the thyroid is incorporated into the metabolic regulators triiodothyronine (T3) and tetraiodothyronine (T4). Mutations in this gene are associated with thyroid dyshormonogenesis 1.

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