Assays & Kits

The Chemi-Verse™ TBK1 Kinase Assay Kit is designed to measure TBK1 (TANK-binding kinase 1) serine/threonine kinase activity for screening and profiling applications using ADP-Glo™ as a detection reagent. The assay kit comes in a convenient 96-well format, with enough recombinant purified TBK1 (amino acids 2-279), kinase substrate, ATP, and kinase assay buffer for 100 enzyme reactions.

The Chemi-Verse™ HER2 Kinase Assay Kit is designed to measure HER2 (human epidermal growth factor receptor 2) tyrosine kinase activity for screening and profiling applications using ADP-Glo™ as a detection reagent. The assay kit comes in a convenient 96-well format, with enough purified HER2 (amino acids 679-1255), kinase substrate, ATP, and kinase assay buffer for 100 enzyme reactions.

The Chemi-Verse™ HER4 Kinase Assay Kit is designed to measure HER4 (human epidermal growth factor receptor 4) tyrosine kinase activity for screening and profiling applications using ADP-Glo™ as a detection reagent. The assay kit comes in a convenient 96-well format, with enough purified HER4 (amino acids 708-993), kinase substrate, ATP, and kinase assay buffer for 100 enzyme reactions.

The Chemi-Verse™ FYN Kinase Assay Kit is designed to measure FYN (FYN proto-oncogene, Src family tyrosine kinase) tyrosine kinase activity for screening and profiling applications using ADP-Glo™ as a detection reagent. The assay kit comes in a convenient 96-well format, with enough purified FYN, kinase substrate, ATP, and kinase assay buffer for 100 enzyme reactions.

The Chemi-Verse™ PIM2 Kinase Assay Kit is designed to measure PIM2 (Proviral Integration of Moloney murine leukemia virus 2) serine/threonine kinase activity for screening and profiling applications using ADP-Glo™ as a detection reagent. The assay kit comes in a convenient 96-well format, with enough purified PIM2, kinase substrate, ATP, and kinase assay buffer for 100 enzyme reactions.

The Chemi-Verse™ Mouse PIM3 Kinase Assay Kit is designed to measure PIM3 (Proviral Integration of Moloney murine leukemia virus 3) serine/threonine kinase activity for screening and profiling applications using ADP-Glo™ as a detection reagent. The assay kit comes in a convenient 96-well format, with enough purified mouse PIM3, kinase substrate, ATP, and kinase assay buffer for 100 enzyme reactions.

The Chemi-Verse™ HCK Kinase Assay Kit is designed to measure human HCK (hematopoietic cell kinase) tyrosine kinase activity for screening and profiling applications using ADP-Glo™ as a detection reagent. The assay kit comes in a convenient 96-well format, with enough purified HCK (amino acids 230-497), kinase substrate, ATP, and kinase assay buffer for 100 enzyme reactions.

Glycogen phosphorylase is divided into active glycogen phosphorylase a (Glycogen phosphorylase a, GPa) and inactive glycogen phosphorylase b (Glycogen phosphorylase b, GPb) two forms. The decomposition of glycogen is mainly carried out under the catalysis of glycogen phosphorylase a. CheKine™ Micro Glycogen Phosphorylase a (GPa) Activity Assay Kit can detect animal tissues, cells or bacteria, plasma, serum or other liquid samples. In this kit, when no activator is added, GPa catalyzes the production of glucose residues from glycogen and inorganic phosphorus to glycogen and glucose 1-phosphate. Under the action of phosphoglucose mutase and 6-phosphate glucose dehydrogenase, it further catalyzes the reduction of NADP to NADPH. Measuring the rate of increase of NADPH at 340 nm can reflect the activity of GPa.

Glycogen phosphorylase is divided into active glycogen phosphorylase a (Glycogen phosphorylase a, GPa) and inactive glycogen phosphorylase b (Glycogen phosphorylase b, GPb) two forms. The decomposition of glycogen is mainly carried out under the catalysis of glycogen phosphorylase a. CheKine™ Micro Glycogen Phosphorylase b (GPb) Activity Assay Kit can detect animal tissues, cells or bacteria, plasma, serum or other liquid samples. In this kit, when no activator is added, GPa catalyzes the production of glucose residues from glycogen and inorganic phosphorus to glycogen and glucose 1-phosphate. Under the action of phosphoglucose mutase and 6-phosphate glucose dehydrogenase, it further catalyzes the reduction of NADP to NADPH. Measuring the rate of increase of NADPH at 340 nm can reflect the activity of GPa. The activity of GP (GPa and GPb) is measured by adding an activator. GPb activity can be obtained by subtracting GPa activity from GP activity