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Rabbit anti-Human APOA2 Polyclonal Antibody

The antibody against APOA2 was raised in rabbit using the Recombinant Human APOA2 fusion protein as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.

ADC-40022A

The antibody against APOA2 was raised in rabbit using the Recombinant Human APOA2 fusion protein as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.

$600.00

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Specifications


Cat.No ADC-40022A ClonalityPolyclonal
Host SpeciesRabbitTarget NameAPOA2
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage BufferPBS with 0.1% sodium azide and 50% glycerol pH 7.3.
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHC, WBStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human APOA2 fusion proteinTarget SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP02652
Background Information
  • Uniprot Id

    P02652

  • Target Species

    Human

  • Target Name

    APOA2

  • Target Full Name

    Apolipoprotein A-II

  • Target Function

    May stabilize HDL (high density lipoprotein) structure by its association with lipids, and affect the HDL metabolism.

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    Apolipoprotein A2 family

  • Target Tissue Specificity

    Plasma; synthesized in the liver and intestine.

  • Target Research Area

    Cancer

  • Target Synonyms

    APO A2; Apo AII; Apo-AII; APOA 2; ApoA II; ApoA-II; APOA2; APOA2_HUMAN; APOAII; Apolipoprotein A II; Apolipoprotein A-II(1-76); Apolipoprotein A2; Apolipoprotein AII; ApolipoproteinA II; OTTHUMP00000032244

  • Target Background

    This gene encodes apolipoprotein (apo-) A-II, which is the second most abundant protein of the high density lipoprotein particles. The protein is found in plasma as a monomer, homodimer, or heterodimer with apolipoprotein D. Defects in this gene may result in apolipoprotein A-II deficiency or hypercholesterolemia.

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