1. The ADP-Glo kinase assay was performed in a solid, white, flat bottom 96-well plate.
2. The reaction volume of 20 µl with 2X 1 µM kinase, 2X 1 µM kinase substrate, and 2X 100 µM ATP in 1X Kinase Reaction Buffer (KRB).
3. The reaction was incubated for an hour at 30°C with gentle shaking.
4. 20 µL of ADP-GLo reagent is added and incubated for 45 minutes.
5. 40 µl of a Kinase Detection Reagent is added to each well and incubated for 60 minutes in the dark.
6. The readout was measured as luminescent values (Relative luminescent unit, RLU).