SKU: 78497489589

UA-Glo® Luminescent Kinase Assay

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Description

UA-Glo® Luminescent Kinase AssayProduct Specification Stability & Storage Dry ice transportation. Store in the dark at 20C or below, with a validity period of 12 months. Background The UA Glo Kinase Luminescent Detection Kit can quantitatively determine the activity of kinases in enzymology experiments. This kit measures kinase activity by quantitatively detecting the amount of remaining ATP after the kinase reaction: the amount of remaining ATP is negatively correlated with kinase

Product Specification


Stability & Storage

Dry ice transportation. Store in the dark at -20°C or below, with a validity period of 12 months.

Background

The UA-Glo Kinase Luminescent Detection Kit can quantitatively determine the activity of kinases in enzymology experiments. This kit measures kinase activity by quantitatively detecting the amount of remaining ATP after the kinase reaction: the amount of remaining ATP is negatively correlated with kinase activity. When using this kit, the maximum ATP concentration in the kinase reaction can reach 10μM; when using the UA-Glo Kinase Plus Luminescent Detection Kit, the maximum ATP concentration in the kinase reaction can reach 100μM; and when using the UA-Glo Kinase Max Luminescent Detection Kit, the maximum ATP concentration in the kinase reaction can reach 500μM. This kit can detect most kinases, and kinase substrates include polypeptides, proteins, lipids, or sugars, etc. The kit can be used for high-throughput homogeneous screening of kinase inhibitors, and can distinguish between ATP-competitive and non-competitive inhibitors by adjusting the ATP concentration.

Components

Product composition: Luciferase, luciferin, and buffer are mixed and filled into 10 ml or 100 ml brown bottles. The specifications are as follows:

Specification

96-well plate reaction count

384-well plate reaction count

10 ml

200

1,000

100 ml

2,000

10,000

10 x 100 ml

20,000

100,000

Protocol

1. Kinase Reaction
1)Perform the kinase reaction in a 96-well or 384-well white opaque assay plate. It is recommended that the reaction volume is 50μL for 96-well plates and 10μL for 384-well plates. Test compounds with concentration gradients can be added to the kinase reaction.
2) The concentrations of kinase and substrate in the kinase reaction need to be optimized according to different kinases. Under the condition of the appropriate signal-to-noise ratio required for the experiment, the kinase concentration within the linear reaction range of the signal can be used for the experiment.
3) Concentration of ATP: The UA-Glo Kinase Luminescent Detection Kit can be used up to 10μM.
4) The kinase reaction can be carried out in a universal reaction buffer (40mM Tris-HCl (pH 7.5), 0.1 mg/ml BSA, 20mM MgCl2) or using reaction buffers and cofactors reported in the literature.
5) The temperature and time of the kinase reaction need to be set according to different kinases. For high-throughput screening experiments of compounds, it is recommended to optimize the kinase reaction to be carried out at room temperature (22℃-25℃) to help maintain the temperature uniformity of the assay plate during the kinase activity determination.

2.  Kinase Activity
1) Take out the UA-Glo Kinase Luminescent Detection Reagent and equilibrate it to room temperature. Mix gently by shaking. The luciferase reaction in the kinase activity luminescent detection reagent is sensitive to temperature changes; the reagent and assay plate need to be equilibrated to room temperature, and the temperature should be kept constant (±1℃) during the test.
2) If the kinase reaction is carried out at a non-room temperature, such as 30℃, the assay plate needs to be equilibrated to room temperature.
3) Add 50 µL of kinase luminescent detection reagent to a 50 µL 96-well assay plate, or 10 µL of kinase luminescent detection reagent to a 10 µL 384-well assay plate, shake to mix, and place in the dark for 10 minutes.
4) Read the fluorescence signal. Since the fluorescence signal is very stable, if necessary, the plate can be read within 3 hours after adding the detection reagent.

Guidelines

1) It is not recommended to arbitrarily change the amount of reaction reagents without strict verification. The volume ratio of the kinase reaction reagent to the UA-Glo kinase luminescent detection reagent should be 1:1.

2) After the first use of the UA-Glo kinase luminescent detection reagent, it should be aliquoted and stored at -20°C to ensure the stability of the reagent. There is no loss of signal intensity after 4 repeated freeze-thaw cycles.

3) This product is for research use only.

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SKU: 78497489589

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