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Rabbit anti-Human SHMT1 Polyclonal Antibody

The antibody against SHMT1 was raised in rabbit using the Recombinant Human Serine hydroxymethyltransferase, cytosolic protein (324-483AA) 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-44339A

The antibody against SHMT1 was raised in rabbit using the Recombinant Human Serine hydroxymethyltransferase, cytosolic protein (324-483AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.

$299.00

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Specifications


Cat.No ADC-44339A ClonalityPolyclonal
Host SpeciesRabbitTarget NameSHMT1
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHC, WBStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Serine hydroxymethyltransferase, cytosolic protein (324-483AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP34896
Background Information
  • Uniprot Id

    P34896

  • Target Species

    Human

  • Target Name

    SHMT1

  • Target Full Name

    Serine hydroxymethyltransferase, cytosolic

  • Target Function

    Interconversion of serine and glycine.

  • Target Subcellular Location

    Cytoplasm.

  • Target Protein Families

    SHMT family

  • Target Synonyms

    CSHMT; Cytoplasmic serine hydroxymethyltransferase; cytosolic; GLYC_HUMAN; Glycine hydroxymethyltransferase; Serine hydroxymethyltransferase 1 (soluble); Serine hydroxymethyltransferase; Serine hydroxymethyltransferase; cytosolic; Serine methylase; SHMT; Shmt1

  • Target Background

    This gene encodes the cytosolic form of serine hydroxymethyltransferase, a pyridoxal phosphate-containing enzyme that catalyzes the reversible conversion of serine and tetrahydrofolate to glycine and 5, 10-methylene tetrahydrofolate. This reaction provides one-carbon units for synthesis of methionine, thymidylate, and purines in the cytoplasm. This gene is located within the Smith-Magenis syndrome region on chromosome 17. A pseudogene of this gene is located on the short arm of chromosome 1. Alternative splicing results in multiple transcript variants.

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