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Recombinant Human Aquaporin-2 (AQP2), Truncated,Yeast

ACP06504

Number
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Specifications


Cat.No ACP06504 Target NameAQP2
Target SynonymsAQP2; Aquaporin-2; AQP-2; ADH water channel; Aquaporin-CD; AQP-CD; Collecting duct water channel protein; WCH-CD; Water channel protein for renal collecting ductFormLiquid or Lyophilized powder
Expression SystemYeastProtein LengthFull length protein
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 IDP41181
Background Information
  • Uniprot Id

    P41181

  • Target Species

    Human

  • Target Name

    AQP2

  • Target Full Name

    Aquaporin-2

  • Target Function

    Forms a water-specific channel that provides the plasma membranes of renal collecting duct with high permeability to water, thereby permitting water to move in the direction of an osmotic gradient. Plays an essential role in renal water homeostasis.

  • Target Involvement

    Diabetes insipidus, nephrogenic, autosomal (ANDI)

  • Target Subcellular Location

    Apical cell membrane; Multi-pass membrane protein. Basolateral cell membrane; Multi-pass membrane protein. Cell membrane; Multi-pass membrane protein. Cytoplasmic vesicle membrane; Multi-pass membrane protein. Golgi apparatus, trans-Golgi network membrane; Multi-pass membrane protein.

  • Target Protein Families

    MIP/aquaporin (TC 1.A.8) family

  • Target Tissue Specificity

    Expressed in collecting tubules in kidney medulla (at protein level). Detected in kidney.

  • Target Research Area

    Signal Transduction

  • Target Synonyms

    AQP2; Aquaporin-2; AQP-2; ADH water channel; Aquaporin-CD; AQP-CD; Collecting duct water channel protein; WCH-CD; Water channel protein for renal collecting duct

  • Target Background

    This gene encodes a water channel protein located in the kidney collecting tubule. It belongs to the MIP/aquaporin family, some members of which are clustered together on chromosome 12q13. Mutations in this gene have been linked to autosomal dominant and recessive forms of nephrogenic diabetes insipidus.

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