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Dual-luciferase Reporter Assay (Dual-LUC)

Clone the regulatory elements of the gene of interest upstream or downstream of the firefly luciferase gene to construct a luciferase reporter plasmid. Then transfect the cells, and after appropriate stimulation or treatment, lyse the cells and measure the luciferase activity. The changes in luciferase activity are used to assess the effects of the stimulation or different treatments on the regulatory elements of interest.
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Description

Why use the dual-luciferase reporter system?

Single-reporter gene experiments are often affected by various experimental conditions. In contrast, the dual-reporter gene system provides a baseline through a co-transfected "control," minimizing the influence of external factors such as cell viability and transfection efficiency on the experiment, making the data more reliable. Typically, the Renilla luciferase gene is used as an internal reference, with both reporter genes constructed on the same plasmid and driven by different promoters. This helps reduce the impact of intrinsic variability, effectively standardizing the experiment and preventing experimental condition changes from interfering with the accuracy of the results. When calculating the results, the value of Firefly luciferase is divided by the value of Renilla luciferase (Firefly luciferase/Renilla luciferase).

 

Service process

Customer places an order online — Order/experimental materials confirmation — Recombinant plasmid preparation — Material selection — Transformation/staining — Cell lysis — Fluorescence detection — Data analysis

 

Delivery time

2 weeks

Our Advantages and Features

  1. Regularly available rice, tobacco, Arabidopsis protoplasts, and tobacco leaves allow for quick experimental results.
  2. Optional pre-experiment for promoter activity detection can be added.
  3. Positive controls are included to ensure the reliability of the experimental process.
  4. In vivo experiments provide a more accurate reflection of interactions within the plant.