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Rabbit anti-Human GNPAT Polyclonal Antibody

The antibody against GNPAT was raised in rabbit using the Synthetic peptide of Human GNPAT as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.

ADC-26655A

The antibody against GNPAT was raised in rabbit using the Synthetic peptide of Human GNPAT as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.

$299.00

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Specifications


Cat.No ADC-26655A ClonalityPolyclonal
Host SpeciesRabbitTarget NameGNPAT
FormLiquidSpecies ReactivityHuman, Mouse, Rat
IsotypeIgGStorage Buffer0.05% NaN3, 40% Glycerol., pH7.4 PBS
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHCStorageUpon receipt

Immunogen Information


Immunogen DescriptionSynthetic peptide of Human GNPATTarget SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDO15228
Background Information
  • Uniprot Id

    O15228

  • Target Species

    Human

  • Target Name

    GNPAT

  • Target Full Name

    Dihydroxyacetone phosphate acyltransferase

  • Target Function

    Dihydroxyacetonephosphate acyltransferase involved in plasmalogen biosynthesis.

  • Target Involvement

    Rhizomelic chondrodysplasia punctata 2 (RCDP2)

  • Target Subcellular Location

    Peroxisome membrane; Peripheral membrane protein; Matrix side.

  • Target Protein Families

    GPAT/DAPAT family

  • Target Synonyms

    Acyl CoA dihydroxyacetonephosphateacyltransferase ; Acyl-CoA:dihydroxyacetonephosphateacyltransferase; DAP AT; DAP-AT; DAPAT; DHAP AT ; DHAP-AT; DHAPAT; Dihydroxyacetone phosphate acyltransferase; EC 2.3.1.42 ; Glycerone-phosphate O-acyltransferase; Glyceronephosphate O acyltransferase; GNPAT; GNPAT_HUMAN; OTTHUMP00000036147

  • Target Background

    This gene encodes an enzyme located in the peroxisomal membrane which is essential to the synthesis of ether phospholipids. Mutations in this gene are associated with rhizomelic chondrodysplasia punctata. Two transcript variants encoding different isoforms have been found for this gene.

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