Light & fluorescence microscopy
Follow the light path, acquire images, and diagnose focus, signal and sampling problems.
Open labA journey into the unseen
There is an extraordinary world
just beyond your sight.
Meet JANA. Your guide to the unseen.
Follow your curiosity from light to atoms.
01 / Change your perspective
Five stops through scale.
A different way to see at every step.
JANA / SCALE NOTES
A cell contains a world of structures. Fluorescence helps distinguish selected features by the light they emit.
Explore light & fluorescence ↗These are comparative illustrations, not a continuous microscope zoom or measurements from a specimen.
Loading the 3D view when it comes into view. You can explore scale using the controls.
02 / Make a discovery
Move through a fluorescent specimen. Separate its channels. Notice what appears—and what disappears.
JANA asks
When a feature disappears, has it gone—or are you looking at a different depth?
CONFOCAL / SYNTHETIC CELLSZ 0.0 µmMove through depth. Watch structures sharpen, soften, or leave the optical section.
Same XY field · fixed display scale · synthetic teaching preview
03 / Follow the light
Open the shutter. Follow the light.
See what each component does.
Explore the LFM simulator’s interactive microscope.
Loads on demand. Drag to orbit; view controls are also available.
The fluorescence journey
Generic teaching model adapted from the LFM simulator. Geometry and light paths are simplified; motion is enlarged for learning. This homepage preview does not capture images or change your lab session.
MICROSCOPY CONCEPTS / LESSON 01
A complete lesson with JANA.
Predict. Experiment. Explain.
Follow the light in 3D. Enlarge two fluorescent points, open the objective aperture, and discover what actually reveals detail.
Start the 3D lessonSAME 300 nm PAIR / 520 nm EMISSION
A smaller Rayleigh reference distance means closer features can meet the criterion. Display zoom alone leaves it unchanged.
The first complete concept lesson. Further topics from magnification and calibration to aberrations and detectors will follow.
04 / From curiosity to practice
One place to learn, practise
and understand your measurements.
Foundations begins with Learn. You can choose any available mode below.
Follow the light path, acquire images, and diagnose focus, signal and sampling problems.
Open labScan a surface and connect probe shape and feedback settings to the measured image.
Open labExplore electron imaging, ion milling and virtual lamella preparation.
Open labExplore the column, specimen loading, beam alignment and image formation.
Open labReconstruct a surface from interference signals and measure step height.
Open labAll five online laboratories are public. Each lab opens in another tab so you can keep your current work. Assessments are available only where implemented; other labs include guided checks and review questions.
05 / New perspectives
Selected research, 2024–2025.
New ideas are changing what we can observe.
A single expansion step enlarged preserved cells and tissues about twentyfold in each dimension, revealing nanoscale biological details with conventional confocal microscopes.
Read the research — Single-shot 20-fold expansion microscopy, Nature MethodsNature Methods · Expansion microscopyRapid electron scanning and computational reconstruction revealed atomic details at fragile perovskite edges, showing what carefully controlled electron dose can make possible.
Read the research — Atomically resolved edges and defects in lead halide perovskites, NatureNature · Low-dose electron imagingA seesaw-shaped probe separated mechanical hinges from its reflective surface, improving deflection sensitivity and capturing proteins and DNA structures in liquid.
Read the research — Seesaw cantilevers for high-speed AFM, Nature CommunicationsNature Communications · Probe designThese are published research advances. They are not claims that MVLscope reproduces these methods.
Your next discovery starts with a question.
JANA guides your journey, from first discoveries to in-lab practice.
JANA / DISCOVERY WINDOW
What becomes easier to distinguish when you separate the signals?
Choose a channel to follow DNA or actin labels through the same synthetic cell field.
Illustrative cell outlines · not a measured specimen.