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Promega™ Kinase-Glo™ Plus Luminescent Kinase Assay System

Homogeneous, high-throughput screening (HTS) method of measuring kinase activity

$155.15 - $4,636.31

Specifications

Format Fluid
For Use With (Application) Automated high throughput screening and they can be used to assay protein, lipid and sugar kinases
Storage Requirements -20°C
View More Specs

 Disclaimers

The method of recombinant expression of Coleoptera luciferase is covered by U.S. Pat. Nos. 5,583,024, 5,674,713 and 5,700,673. A license (from Promega for research reagent products and from The Regents of the University of California for all other fields) is needed for any commercial sale of nucleic acid contained within or derived from this product.

Products
Catalog Number Mfr. No. Quantity pH Price Quantity    

PR-V3774

 
promega™
V3774
10 × 100mL 7 Each for $4,636.31

PR-V3771

 
promega™
V3771
10mL 7 Each for $155.15

PR-V3772

 
promega™
V3772
10 × 10mL 7 Each for $704.06

PR-V3773

 
promega™
V3773
100mL 7 Each for $602.41
Description & Specifications

Specifications

Format Fluid
For Use With (Application) Automated high throughput screening and they can be used to assay protein, lipid and sugar kinases
Storage Requirements -20°C

Quantifies amount of ATP remaining in solution following a kinase reaction. Easily performed in a single well of a 96- or 384-well plate: simply add volume of Kinase-Glo Plus reagent equal to volume of completed kinase reaction, then measure luminescence.

  • Ideal for high-throughput analysis of library compounds to identify kinase inhibitors
  • Compatible with virtually any kinase/kinase substrate combination
  • Can be performed at higher ATP concentrations than traditional Kinase-Glo assay
  • Suitable for screening non-ATP binding site inhibitors: Kinase-Glo Plus Assay is linear to 100μM ATP, making it well-suited for use with kinases with high Km for ATP as well as for screening for kinase inhibitors that do not compete at the ATP binding site
  • Can be used for a wide variety of kinases (lipid, sugar, and alcohol) and substrates (peptides, proteins, lipids, sugars, alcohols)
  • Less susceptible to interference than traditional luciferase-based ATP detection reagents
  • Nonradioactive