PDE4D2 Assay Kit

Catalog #
60345
$455 *
Size: 96 reactions
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Description

The PDE4D2 Assay Kit is designed for identification of inhibitors of PDE4D2 using fluorescence polarization. The assay is based on the binding of a fluorescent nucleotide monophosphate generated by PDE4D2 to the binding agent. The key to the PDE4D2 Assay Kit is the specific binding agent. Using this kit, only two simple steps on a microtiter plate are required for PDE4D2 reactions. First, the fluorescently labeled cAMP is incubated with a sample containing PDE4D2 for 1 hour. Second, a binding agent is added to the reaction mix to produce a change in fluorescent polarization that can then be measured using a fluorescence reader equipped for the measurement of fluorescence polarization.

Need us to run inhibitor screens or profile your compounds against PDE4D2? Check out our Phosphodiesterase Screening Services.

This product has been cited 9 times.

Synonyms
inhibitor screening, assay kit, PDE4D, PDE4-D2, PDE
Product Info
Storage and Usage
Citations9
Assay Kit Format
Fluorescence Polarization
Supplied As
The PDE4D2 Assay Kit comes in a convenient 96-well format, with purified PDE4D2enzyme, fluorescently labeled PDE4D substrate (cAMP), binding agent, and PDE assaybuffer for 100 enzyme reactions.
Format

UniProt #
Q08499-5
Background
Phosphodiesterases (PDEs) play an important role in the dynamic regulation of cAMP and cGMP signaling. PDE4D is a regulator of airway smooth-muscle contractility, and has been identified as a potential risk predictor for ischemic stroke. Additionally, PDE4D has been associated with asthma pathophysiology and bone formation. The PDE4D gene encodes at least 9 different isoforms. Phosphodiesterases catalyze the hydrolysis of the phosphodiester bond in dye-labeled cyclic monophosphates. Beads selectively bind the phosphate group in the nucleotide product. This increases the size of the nucleotide relative to unreacted cyclic monophosphate. In the polarization assay, dye molecules with absorption transition vectors parallel to the linearly-polarized excitation light are selectively excited. Dyes attached to the rapidly-rotating cyclic monophosphates will obtain random orientations and emit light with low polarization. Dyes attached to the slowly-rotating nucleotide-bead complexes will not have time to reorient and therefore will emit highly polarized light.
References

Chandrasekaran A, et al., Cell Signal. 2008;20(1):139-53.