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Recombinant Human Iodotyrosine dehalogenase 1 (IYD), Truncated

ACP16110

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP16110 Target NameIYD
Target SynonymsIYD; C6orf71; DEHAL1; Iodotyrosine deiodinase 1; IYD-1; EC 1.21.1.1; Iodotyrosine dehalogenase 1FormLyophilized 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 IDQ6PHW0
Background Information
  • Uniprot Id

    Q6PHW0

  • Target Species

    Human

  • Target Name

    IYD

  • Target Full Name

    Iodotyrosine deiodinase 1

  • Target Function

    Catalyzes the oxidative NADPH-dependent deiodination of monoiodotyrosine (L-MIT) or diiodotyrosine (L-DIT). Acts during the hydrolysis of thyroglobulin to liberate iodide, which can then reenter the hormone-producing pathways. Acts more efficiently on monoiodotyrosine than on diiodotyrosine.

  • Target Involvement

    Thyroid dyshormonogenesis 4 (TDH4)

  • Target Subcellular Location

    Cell membrane; Single-pass membrane protein. Cytoplasmic vesicle membrane.

  • Target Protein Families

    Nitroreductase family

  • Target Tissue Specificity

    Expressed at a high level in thyroid gland (at protein level). Expressed at a high level in thyroid gland and at lower level in kidney and trachea.

  • Target Synonyms

    IYD; C6orf71; DEHAL1; Iodotyrosine deiodinase 1; IYD-1; EC 1.21.1.1; Iodotyrosine dehalogenase 1

  • Target Background

    This gene encodes an enzyme that catalyzes the oxidative NADPH-dependent deiodination of mono- and diiodotyrosine, which are the halogenated byproducts of thyroid hormone production. The N-terminus of the protein functions as a membrane anchor. Mutations in this gene cause congenital hypothyroidism due to dyshormonogenesis type 4, which is also referred to as deiodinase deficiency, or iodotyrosine dehalogenase deficiency, or thyroid hormonogenesis type 4. Alternative splicing results in multiple transcript variants.

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