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Recombinant Human S-adenosylmethionine synthase isoform type-1 (MAT1A)

ACP00310

Number
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Specifications


Cat.No ACP00310 Target NameMAT1A
Target SynonymsAdoMet synthase 1;Methionine adenosyltransferase 1(MAT 1);Methionine adenosyltransferase I/III(MAT-I/III)FormLiquid or Lyophilized powder
Expression SystemE.coliExpression Range1-395aa
Mol Weight47.3Protein LengthFull length
PurityGreater than 90% as determined by SDS-PAGE.Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDQ00266
Background Information
  • Uniprot Id

    Q00266

  • Target Species

    Human

  • Target Name

    MAT1A

  • Target Full Name

    S-adenosylmethionine synthase isoform type-1

  • Target Function

    Catalyzes the formation of S-adenosylmethionine from methionine and ATP. The reaction comprises two steps that are both catalyzed by the same enzyme: formation of S-adenosylmethionine (AdoMet) and triphosphate, and subsequent hydrolysis of the triphosphate.

  • Target Involvement

    Methionine adenosyltransferase deficiency (MATD)

  • Target Protein Families

    AdoMet synthase family

  • Target Tissue Specificity

    Expressed in liver.

  • Target Research Area

    Signal Transduction

  • Target Synonyms

    MAT1A; AMS1; MATA1S-adenosylmethionine synthase isoform type-1; AdoMet synthase 1; EC 2.5.1.6; Methionine adenosyltransferase 1; MAT 1; Methionine adenosyltransferase I/III; MAT-I/III

  • Target Background

    This gene catalyzes a two-step reaction that involves the transfer of the adenosyl moiety of ATP to methionine to form S-adenosylmethionine and tripolyphosphate, which is subsequently cleaved to PPi and Pi. S-adenosylmethionine is the source of methyl groups for most biological methylations. The encoded protein is found as a homotetramer (MAT I) or a homodimer (MAT III) whereas a third form, MAT II (gamma), is encoded by the MAT2A gene. Mutations in this gene are associated with methionine adenosyltransferase deficiency.

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