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Rabbit anti-Human RARS2 Polyclonal Antibody

The antibody against RARS2 was raised in rabbit using the Recombinant Human Probable arginine--tRNA ligase, mitochondrial protein (17-340AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.

ADC-16631A

The antibody against RARS2 was raised in rabbit using the Recombinant Human Probable arginine–tRNA ligase, mitochondrial protein (17-340AA) 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-16631A ClonalityPolyclonal
Host SpeciesRabbitTarget NameRARS2
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHCStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Probable arginine--tRNA ligase, mitochondrial protein (17-340AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ5T160
Background Information
  • Uniprot Id

    Q5T160

  • Target Species

    Human

  • Target Name

    RARS2

  • Target Full Name

    Probable arginine--tRNA ligase, mitochondrial

  • Target Involvement

    Pontocerebellar hypoplasia 6 (PCH6)

  • Target Subcellular Location

    Mitochondrion matrix.

  • Target Protein Families

    Class-I aminoacyl-tRNA synthetase family

  • Target Synonyms

    arginine tRNA ligase; arginyl tRNA synthetase 2 mitochondrial; Arginyl tRNA synthetase; Arginyl-tRNA synthetase; ArgRS; DALRD2; mitochondrial; PCH6; Probable arginine tRNA ligase; probable arginine tRNA ligase mitochondrial; Probable arginine--tRNA ligase; probable arginyl tRNA synthetase mitochondrial; RARS2; RARSL; SYRM_HUMAN

  • Target Background

    This nuclear gene encodes a protein that localizes to the mitochondria, where it catalyzes the transfer of L-arginine to its cognate tRNA, an important step in translation of mitochondrially-encoded proteins. Defects in this gene are a cause of pontocerebellar hypoplasia type 6 (PCH6). Alternative splicing results in multiple transcript variants.

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