The Kinase Enzyme Systems include a recombinant kinase enzyme, a substrate appropriate for the enzyme, a reaction buffer and supplemental reagents as needed. The DGKQ Kinase Enzyme System contains:
- DGKQ Kinase, 10μg (Human, recombinant, full-length);. MW: ~130kDa
- Dilauroyl-sn-glycerol Substrate, 10mM
- 5X Reaction Buffer; DTT, 0.1M; Lipid Dilution Buffer II
Recombinant full-length human DGKQ was expressed by baculovirus in Sf9 insect cells using an N-terminal GST tag. Diacylglycerol kinase theta (DAG kinase theta) is the only member of class V diacylglycerol kinase, which contains three cysteine-rich domains, a proline-rich region, and a Ras-associating domain and mediates the regeneration of phosphatidylinositol from diacylglycerol in cell signal transduction. DGKQ has been associated with Parkinson’s disease in a genome-wide meta-analysis study. Stimulated DGK theta activity promotes the SF1-dependent transcription of CYP17 in human adrenocortical cells.
Application Note
NCBI Database Entry
The DGKQ Kinase Enzyme System can be purchased with or without the ADP-Glo™ Kinase Assay reagents. Used together, the ADP-Glo™ Kinase Assay + Kinase Enzyme Systems provide a convenient method for profiling the effect of lead compounds on kinase activity. Assay advantages include broad dynamic range, ease of use and high sensitivity. Kinase Enzyme Systems are manufactured by SignalChem. Bulk quantities available upon request.
Use with ADP-Glo™ Kinase Assay
The ADP-Glo™ Kinase Assay is a luminescent kinase assay that measures ADP formed from a kinase reaction; ADP is converted into ATP, which is a substrate in a reaction catalyzed by Ultra-Glo™ Luciferase that produces light. The luminescent signal positively correlates with ADP amount and kinase activity. The assay is well suited for measuring the effects of chemical compounds on the activity of a broad range of purified kinases, making it ideal for both primary screening as well as kinase selectivity profiling. The ADP-Glo™ Kinase Assay can be used to monitor the activity of virtually any ADP-generating enzyme (e.g., kinase or ATPase) using up to 1mM ATP.