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Rabbit anti-Human GCSH Polyclonal Antibody

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

ADC-48479A

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

$600.00

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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ADC-48479A ClonalityPolyclonal
Host SpeciesRabbitTarget NameGCSH
Target SynonymsGCSHGlycine cleavage system H protein antibody; mitochondrial antibody; Lipoic acid-containing protein antibodyFormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, Avoid freeze / thaw cycles., PBS with 0.1% Sodium AzidePurification MethodAntigen affinity purified
ConjugateNon-conjugatedApplicationELISA, IF, IHC, WB
StorageUpon receipt

Immunogen Information


Immunogen DescriptionHuman GCSHTarget SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP23434
Background Information
  • Uniprot Id

    P23434

  • Target Species

    Human

  • Target Name

    GCSH

  • Target Full Name

    Glycine cleavage system H protein, mitochondrial

  • Target Function

    The glycine cleavage system catalyzes the degradation of glycine. The H protein (GCSH) shuttles the methylamine group of glycine from the P protein (GLDC) to the T protein (GCST).

  • Target Involvement

    Non-ketotic hyperglycinemia (NKH)

  • Target Subcellular Location

    Mitochondrion.

  • Target Protein Families

    GcvH family

  • Target Synonyms

    GCSHGlycine cleavage system H protein; mitochondrial; Lipoic acid-containing protein

  • Target Background

    Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the H protein, which transfers the methylamine group of glycine from the P protein to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH). Two transcript variants, one protein-coding and the other probably not protein-coding, have been found for this gene. Also, several transcribed and non-transcribed pseudogenes of this gene exist throughout the genome.

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