PDE8A Assay Kit

Catalog #
60380
$405 *
Size: 96 reactions
Qty
*US Pricing only. For international pricing, please contact your local distributor.
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Description

The PDE8A Assay Kit is designed for identification of PDE8A inhibitors using fluorescence polarization. The assay is based on the binding of a fluorescent nucleotide monophosphate generated by PDE8A to the binding agent. The key to the PDE8A Assay Kit is the specific binding agent. Using this kit, only two simple steps on a microtiter plate are required for PDE8A reactions. First, the fluorescently labeled cAMP is incubated with a sample containing PDE8A for 1 hour. Second, a binding agent is added to the reaction mix to produce a change in fluorescent polarization. The FP signal is measured using a fluorescent microplate reader capable of measuring fluorescence polarization.

Need us to run inhibitor screens or profile your compounds against PDE8A? Check out our Phosphodiesterase Screening Services.

Synonyms
inhibitor screening, assay kit, PDE8A, PDE8-A, PDE
Product Info
Storage and Usage
Citations
Assay Kit Format
Fluorescence Polarization
Species
Human
Supplied As
The PDE8A inhibitor screening assay kit comes in a convenient 96-well format,including purified PDE8A enzyme, fluorescently labeled PDE8A substrate (cAMP),binding agent, and PDE assay buffer for 100 enzyme reactions.
Format

Catalog #

Component

Amount

Storage

60080

PDE8A1 recombinant enzyme

>1 µg

-80°C

(Avoid freeze/ thaw cycles!)

60200

FAM-Cyclic-3′, 5′-AMP: 20 µM

50 µl

-80°C

60393 

PDE assay buffer

25 ml

-20°C

60390 

Binding Agent

100 µl

+4°C

60391

Binding Agent Diluent (cAMP)

10 ml

+4°C

79685

Black, low binding, microtiter plate

1

Room temp.

UniProt #
O60658
Background
Phosphodiesterases (PDEs) play an important role in the dynamic regulation of cAMP and cGMP signaling. PDE8 is involved in many biological processes, including T-cell activation, testosterone production, adrenocortical hyperplasia, and thyroid function. 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
Wang, H., et al. Biochemistry 2008; 48: 12760-8.