Methionine Adenosyltransferase (MAT) activity assay kit

Methionine Adenosyltransferase (MAT) activity assay kit

Catalog Number:
EAK1237987ART
Mfr. No.:
IK00403
Price:
$878
  • Size:
    48 tests
    Quantity:
    Add to Cart:
      • Overview
        • Except for parasites that rely on host for living, cells from all organisms have methionine adenyltransferase (MAT, EC2.5.1.6), also known as S­adenosylmethionine synthetase. MAT genes have been found to be exceptionally conserved throughout evolution. It was reported that there is 59% homology between human and E. coli MAT gene sequences. In mammals, three forms or isozymes of MAT have been identified that are encoded by three MAT genes. The MAT1a gene encodes a1 catalytic subunit. MAT-I is a tetramer of a1 subunits and MAT-Ill a dimer of the same subunits. Both MAT-I and MAT-Ill are present in adult liver cells. MAT-II is a heterotetramer formed by MAT2a encoding the catalytic subunit of a2 and MAT2b gene encoding regulatory 13 subunit, present in cells other than liver,embryonic liver and hepatoma cells. MAT catalytic reaction in the body is divided into two steps: (1) Catalyze L-methionine (L-Met) and adenosine triphosphate (ATP) to generate S­adenosylmethionine (known as the active methionine, SAM) and tripolyphosphate (PPPi). Both SAM and PPPi remain on the surface of MAT at this stage. (2)The phosphatase activity of MAT further decompose PPPi to dimeric phosphoric acid (PPi) and inorganic monophosphate (Pi). SAM can only be synthesized by MAT. SAM is one of the few sulfur-containing active substances that carry extremely diverse and important biological functions in nature and is the key molecules in the methionine cycle.

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      • Properties
        • Storage
          Except for the HRP substrate and stop solution that are stored at 2-8°C, all other ingredients and strips can be frozen stored.

          * For research use only

      • Applications
        • Application
          Activity Assay
          Application Description
          This assay kit is designed to calculate MAT activity through measuring the concentration of the main product SAM. The chemical reaction and the competition enzyme-linked immune-absorbent assay (cELISA) are carried out simultaneously, so that the SAM synthesized from the chemical reaction competes with antigens coated on the micro-titer plate for the horseradish peroxidase (HRP) -conjugated anti-SAM antibody the minute it is generated. The SAM is quantified based on the amount of the HRP-anti-SAM antibodies that was made not to bind to the micro-titer plate.

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