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GIPR Recombinant Monoclonal Antibody

The recombinant antibody against GIPR was produced using the Recombinant Human GIPR protein as the immunogen. This antibody exists as a non-conjugated isotype Human IgG, Affinity-chromatography purified. This antibody has been validated on ELISA, WB.

ADC-56377A

The recombinant antibody against GIPR was produced using the Recombinant Human GIPR protein as the immunogen. This antibody exists as a non-conjugated isotype Human IgG, Affinity-chromatography purified. This antibody has been validated on ELISA, WB.

$350.00

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Specifications


Cat.No ADC-56377A ClonalityMonoclonal
Target NameGIPRTarget SynonymsGastric inhibitory polypeptide receptor, GIPR
FormLiquidSpecies ReactivityHuman
IsotypeHuman IgGStorage Buffer0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4
Purification MethodAffinity-chromatography purifiedConjugateNon-conjugated
ApplicationELISA, WBStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human GIPR proteinTarget SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP48546
Background Information
  • Uniprot Id

    P48546

  • Target Species

    Human

  • Target Name

    GIPR

  • Target Full Name

    Gastric inhibitory polypeptide receptor

  • Target Function

    This is a receptor for GIP. The activity of this receptor is mediated by G proteins which activate adenylyl cyclase.

  • Target Subcellular Location

    Cell membrane; Multi-pass membrane protein.

  • Target Protein Families

    G-protein coupled receptor 2 family

  • Target Research Area

    Others

  • Target Synonyms

    GIPR; Gastric inhibitory polypeptide receptor; GIP-R; Glucose-dependent insulinotropic polypeptide receptor

  • Target Background

    This gene encodes a G-protein coupled receptor for gastric inhibitory polypeptide (GIP), which was originally identified as an activity in gut extracts that inhibited gastric acid secretion and gastrin release, but subsequently was demonstrated to stimulate insulin release in the presence of elevated glucose. Mice lacking this gene exhibit higher blood glucose levels with impaired initial insulin response after oral glucose load. Defect in this gene thus may contribute to the pathogenesis of diabetes.

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