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Recombinant Human Transferrin receptor protein 2 (TFR2), Truncated

ACP09994

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP09994 Target NameTFR2
Target SynonymsHFE 3; HFE3; MGC126368; TFR 2; TfR2; TFR2_HUMAN; TFRC 2; TFRC2; Transferrin receptor 2; Transferrin receptor protein 2FormLyophilized 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 IDQ9UP52
Background Information
  • Uniprot Id

    Q9UP52

  • Target Species

    Human

  • Target Name

    TFR2

  • Target Full Name

    Transferrin receptor protein 2

  • Target Function

    Mediates cellular uptake of transferrin-bound iron in a non-iron dependent manner. May be involved in iron metabolism, hepatocyte function and erythrocyte differentiation.

  • Target Involvement

    Hemochromatosis 3 (HFE3)

  • Target Subcellular Location

    Cell membrane; Single-pass type II membrane protein.; [Isoform Beta]: Cytoplasm. Note=Lacks the transmembrane domain. Probably intracellular.

  • Target Protein Families

    Peptidase M28 family, M28B subfamily

  • Target Tissue Specificity

    Predominantly expressed in liver. While the alpha form is also expressed in spleen, lung, muscle, prostate and peripheral blood mononuclear cells, the beta form is expressed in all tissues tested, albeit weakly.

  • Target Synonyms

    HFE 3; HFE3; MGC126368; TFR 2; TfR2; TFR2_HUMAN; TFRC 2; TFRC2; Transferrin receptor 2; Transferrin receptor protein 2

  • Target Background

    This gene encodes a single-pass type II membrane protein, which is a member of the transferrin receptor-like family. This protein mediates cellular uptake of transferrin-bound iron, and may be involved in iron metabolism, hepatocyte function and erythrocyte differentiation. Mutations in this gene have been associated with hereditary hemochromatosis type III. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.

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