IMAP® FP Kinase, Phosphatase, and Phosphodiesterase Assays by Molecular Devices®
Manufacturer Molecular Devices®
Homogeneous assay for accurate determination of kinase, phosphatase, and phosphodiesterase activities IMAP® technology provides a homogeneous assay applicable to a wide variety of kinases without regard for substrate peptide sequence. The assay is a simple ""mix-and-read"" procedure that allows accurate determination of kinase, phosphatase, and phosphodiesterase (PDE) activity. Based on the specific, high-affinity interaction of trivalent metal-containing nanoparticles with phosphogroups, IMAP i... Read more
IMAP® FP Kinase, Phosphatase, and Phosphodiesterase Assays
Homogeneous assay for accurate determination of kinase, phosphatase, and phosphodiesterase activities
IMAP® technology provides a homogeneous assay applicable to a wide variety of kinases without regard for substrate peptide sequence. The assay is a simple ""mix-and-read"" procedure that allows accurate determination of kinase, phosphatase, and phosphodiesterase (PDE) activity.
Based on the specific, high-affinity interaction of trivalent metal-containing nanoparticles with phosphogroups, IMAP is a generic platform to assess kinase, phosphatase, and phosphodiesterase activity. An enzyme reaction is performed using fluorescently labeled substrate. Addition of the IMAP Binding System stops the enzyme reaction and specifically binds the phosphorylated substrates. Binding of the substrate to the beads can be detected using either FP or TR-FRET as a readout.
IMAP® technology provides a homogeneous assay applicable to a wide variety of kinases without regard for substrate peptide sequence. The assay is a simple ""mix-and-read"" procedure that allows accurate determination of kinase, phosphatase, and phosphodiesterase (PDE) activity.
Based on the specific, high-affinity interaction of trivalent metal-containing nanoparticles with phosphogroups, IMAP is a generic platform to assess kinase, phosphatase, and phosphodiesterase activity. An enzyme reaction is performed using fluorescently labeled substrate. Addition of the IMAP Binding System stops the enzyme reaction and specifically binds the phosphorylated substrates. Binding of the substrate to the beads can be detected using either FP or TR-FRET as a readout.
Product Overview
IMAP® FP Kinase, Phosphatase, and Phosphodiesterase Assays
Manufacturer Molecular Devices®
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