Why Pay More for TR-FRET Assays?
Enhanced TR-FRET Made Simple
|
Thunder™ uses an optimized donor–acceptor pair (Europium + Far-Red fluorophore) to deliver:
✅ Optimized antibody concentrations ensure superior S/B ratios vs. standard TR-FRET assays. |
|||||||||||||||
Cryopreserved Format = Total Flexibility
Forget the hassle of long-term cell maintenance. With Transiport cells:
- Cells are readily available when you need them
- Assay prep is fast and straightforward - just thaw, seed, and go
- Use normal condition culture (5 % CO2, humidity), no need to block an incubator at 8% or low humidity
- Complete your experiment in as little as two days
This streamlined workflow lets you plan experiments on your schedule, without compromising on data quality.
Built-In Accuracy: Ratiometric Measurement for Reliable Results
Another major advantage of TR-FRET is the ability to analyze data not only from the 665 nm emission signal, but also using the 665/615 nm ratio. This ratiometric measurement improves reproducibility by correcting small pipetting errors and minimizing compound-related artifacts.
Some test compounds may reduce the donor signal at 615 nm (for example, through light absorption, scattering, or the inner filter effect). By using the 665/615 nm ratio, Thunder™ TR-FRET automatically compensates for these issues, ensuring cleaner, more reliable assay results.
![]() |
Figure 1: The binding of Eu-labeled and FR-labeled antibodies to the target protein in the cell lysate brings donor and acceptor molecules into close proximity. Upon excitation of the Europium chelate at 320 or 340 nm, energy is transferred to the far-red acceptor fluorophore, which in turn emits light at 665 nm. The intensity of light emission at 665 nm is proportional to the level of protein. |
|||||
Proven in Cellular Signaling Assays
Thunder™ is validated in real-world cell models, showing robust performance and competitive advantage:
|
Phospho-IRβ (Y1150/Y1151) in B lymphocytes
|
Phospho-ERK1/2 (T202/Y204) in HEK293 cells
|
|
|
|
|
Figure 2: Modulation of phospho-Insulin Receptor β (Y1150/Y1151) in B lymphocyte cells. |
Figure 3: Stimulation of phospho-ERK1/2 (T202/Y204) in HEK293 cells |
These results give scientists the confidence to adopt Thunder™ for routine screening.
Why Choose Thunder™ with Tebubio: Trusted Science. Smarter Pricing.
Compared to competitors kits, Thunder™ offers:
- Same assay performance, 30–40% more cost-effective
- Flexible pack sizes (100 to 20.000 points) → adapt to your projects
- Novel assays covering targets not always addressed by competitors
- Supported by Tebubio’s scientific experts in Europe
Adopt Thunder™ as your TR-FRET solution and stretch your R&D budget further.
-
References
Image: Coutesy of BioAuxilium, your trusted partner for Förster resonance energy transfer technology.
See the Results for Yourself
Ready to try Thunder™ TR-FRET? Join leading scientists already using Thunder™ for routine, reproducible assays.
Order your kit today and experience the same reliability, with sustainable pricing.




