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Methionine Adenosyltransferase Activity Assay Kit (Colorimetric)

Measurement of MAT activity in complex biological matrices
Catalog #: K2033
$625.00

Product Details

Cat # +Size K2033-100
Size 100 assays
Detection Method Absorbance 570 nm
Species Reactivity All
Applications Rapid assessment of MAT activity in biological samples or recombinant MAT preparations
Features & Benefits • The limit of quantification of 2 mU MAT activity per well
• The assay is high-throughput adaptable
• Simple to perform
• Does not require complicated sample processing
• The assay is homogeneous
Kit Components • MAT Assay Buffer
• MAT Probe
• MAT Substrate Mix
• Detection Enzyme Mix
• Detection Cofactor Mix
• Developer Mix
• MAT Positive Control
• Pyrophosphate Standard
Storage Conditions -20ºC
Shipping Conditions Gel Pack
USAGE For Research Use Only! Not For Use in Humans.

Details

Methionine Adenosyltransferases (MATs, EC 2.5.1.6), also known as Adenosylmethionine Synthetases are a family of enzymes that synthesize S-adenosyl-L-methionine (SAMe) from L-methionine and ATP. SAMe is a primary biochemical alkylation agent (one of only two possible methyl group donors) and is also a vital metabolic precursor of the transsulfuration and polyamine synthesis (aminopropylation) pathways. All organisms express at least one MAT enzyme. In mammals, three isozymes of MAT have been identified. MAT1 and MAT3 isozymes are predominantly expressed in the liver, whereas MAT2A is expressed in most tissues. Upregulation of the MAT2A isozyme has been linked to several human diseases. MAT2A has become a popular drug target for novel cancer therapeutics as well as for hepatic fibrosis and non-alcoholic fatty liver disease. BioVision’s Methionine Adenosyltransferase Activity Assay Kit enables the rapid measurement of MAT activity in complex biological matrices. The assay is based on the detection of pyrophosphate, which is generated stoichiometrically during the generation of SAMe. Pyrophosphate is enzymatically metabolized to an intermediate product, which reacts with the probe to form a stable chromophore that is detected by absorbance at 570 nm. The assay is homogeneous, simple to perform and does not require complicated sample processing. The assay is high-throughput adaptable and has a limit of quantification of 2 mU MAT activity per well.


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