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Rabbit anti-Human ADORA2B Polyclonal Antibody, Biotin conjugated

The antibody against ADORA2B was raised in rabbit using the Recombinant Human Adenosine receptor A2b protein (292-332AA) as the immunogen. This antibody exists as a biotin conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA.

ADC-14096A

The antibody against ADORA2B was raised in rabbit using the Recombinant Human Adenosine receptor A2b protein (292-332AA) as the immunogen. This antibody exists as a biotin conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA.

$299.00

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Specifications


Cat.No ADC-14096A ClonalityPolyclonal
Host SpeciesRabbitTarget NameADORA2B
Target SynonymsADORA2B; Adenosine receptor A2bFormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4Purification Method>95%, Protein G purified
ConjugateBiotin conjugatedApplicationELISA
StorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Adenosine receptor A2b protein (292-332AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP29275
Background Information
  • Uniprot Id

    P29275

  • Target Species

    Human

  • Target Name

    ADORA2B

  • Target Full Name

    Adenosine receptor A2b

  • Target Function

    Receptor for adenosine. 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 1 family

  • Target Synonyms

    ADORA2B; Adenosine receptor A2b

  • Target Background

    This gene encodes an adenosine receptor that is a member of the G protein-coupled receptor superfamily. This integral membrane protein stimulates adenylate cyclase activity in the presence of adenosine. This protein also interacts with netrin-1, which is involved in axon elongation. The gene is located near the Smith-Magenis syndrome region on chromosome 17.

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