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Recombinant Human Hereditary hemochromatosis protein (HFE), Truncated

ACP02375

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP02375 Target NameHFE
FormLiquid or Lyophilized powderExpression SystemE.coli
Expression Range23-306aaMol Weight40.2 kDa
Protein LengthExtracellular DomainPurityGreater than 85% as determined by 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 IDQ30201
Background Information
  • Uniprot Id

    Q30201

  • Target Species

    Human

  • Target Name

    HFE

  • Target Full Name

    Hereditary hemochromatosis protein

  • Target Function

    Binds to transferrin receptor (TFR) and reduces its affinity for iron-loaded transferrin.

  • Target Involvement

    Hemochromatosis 1 (HFE1); Variegate porphyria (VP); Microvascular complications of diabetes 7 (MVCD7)

  • Target Subcellular Location

    Cell membrane; Single-pass type I membrane protein.

  • Target Protein Families

    MHC class I family

  • Target Tissue Specificity

    Expressed in all tissues tested except brain.

  • Target Research Area

    Metabolism

  • Target Synonyms

    dJ221C16.10.1; Hemochromatosis; Hemochromatosis protein; Hereditary hemochromatosis protein; Hereditary hemochromatosis protein HLA H; HFE 1; HFE; HFE_HUMAN; HFE1; HH; High Fe; HLA H; HLA-H; HLAH; MGC:150812; MGC10379; MGC103790; MHC class I like protein HFE; MVCD7; TFQTL2

  • Target Background

    The protein encoded by this gene is a membrane protein that is similar to MHC class I-type proteins and associates with beta2-microglobulin (beta2M). It is thought that this protein functions to regulate iron absorption by regulating the interaction of the transferrin receptor with transferrin. The iron storage disorder, hereditary haemochromatosis, is a recessive genetic disorder that results from defects in this gene.

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