Frequently Asked Questions
GloMax® Galaxy Bioluminescence Imager
The complete protocol for this product is available in Technical Manual #TM756.
Considering live-cell imaging? Here’s what you need to know about getting started with the GloMax® Galaxy Bioluminescence Imager.
What is the GloMax® Galaxy Bioluminescence Imager designed for?
What applications does the GloMax® Galaxy Bioluminescence Imager support?
The system is ideal for:
- Validating NanoLuc®-based assays (e.g., NanoBiT, NanoBRET, Nano-Glo)
- Visualizing protein localization and degradation
- Tracking live-cell kinetics over time
- Confirming assay results from a plate reader using spatial imaging.
Want to explore a full array of applications? View the GloMax® Galaxy Application Hub.
How do I choose the right NanoLuc® technology for live-cell imaging?
The right technology depends on the biology you want to observe:
- Use NanoBiT® technology for protein-protein interaction studies.
- Use HiBiT to monitor endogenous protein levels and localization.
- Use NanoBRET® technology to track molecular engagement or trafficking events.
These are compatible with live-cell formats and produce bioluminescent signals well-suited for imaging with the GloMax® Galaxy Bioluminescence Imager. Select an assay that gives a durable signal and minimal perturbation to the system you're studying.
Which NanoLuc® Substrate should I use?
- For end-point experiments: Prioritize signal intensity with Nano-Glo® Live Cell Assay System for maximum brightness when kinetic imaging is not required.
- For kinetic real-time imaging: Prioritize stability with the use of Nano-Glo® Vivazine® or Endurazine™ for tracking protein dynamics over hours.
Is this instrument compatible with fluorescent imaging too?
How does bioluminescence compare to fluorescence for imaging?
See also: Bioluminescence vs. Fluorescence
What should I consider before starting a live-cell bioluminescence imaging experiment?
What labware is compatible with the system?
How do I optimize bioluminescence exposure timing?
What tips can help optimize signal quality?
- Use media without phenol red to reduce background.
- Maintain proper cell seeding density (e.g., 1 × 10? cells/mL).
- Ensure proper cell adherence to the plate/vessel bottom to improve image focus.
- Choose long-lived substrates like Endurazine™ or Vivazine™ for extended imaging windows. Consider using binning (2x2 or 4x4) to boost sensitivity for low-abundance proteins. Binning combines neighboring pixels to boost signal brightness when imaging faint targets.
Can I analyze the images in ImageJ/Fiji?
What are common pitfalls in live-cell imaging, and how can I avoid them?
- Low signal intensity: Confirm proper substrate concentration and avoid over-dilution. Use binning to boost sensitivity if needed. Test several exposure times.
- High background: Use phenol red–free media and ensure the imaging vessel is clean and properly seated.
- Cell health issues during imaging: Avoid overexposure and excitation-based methods when possible. For long-term experiments, use long-lived substrates and minimize temperature fluctuation.
- Drifting focus: Make sure the vessel matches the selected imaging protocol and is seated flat on the stage. Ensure your cells are adhered to the plate bottom with brightfield imaging.
Want more help with your live cell imaging experiments? Consider reading our white paper: How To Image Live-Cell Assays on GloMax® Galaxy Bioluminescence Imager
The GloMax® Galaxy Bioluminescence Imager is a Research Use Only Device. Not for Use in Diagnostic Procedures.
For additional information, view the GloMax® Galaxy Bioluminescence Imager product page.
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