Resources
Here are two tables to help you select the confocal microscope that best suits your imaging needs
1- Microscope selection by application
2- Microscope selection by imaging technique
Please Note:
Application Area | Type of Experiment | BC43 | Dragonfly 200 | Dragonfly 600 |
Cell Biology | Intracellular Structure | |||
Cell Cycle - Cell Division | ||||
Mitochondria Imaging (fixed) | ||||
Cytokinesis | ||||
Mitochondria Imaging (live) | ||||
Early Embryo Development | ||||
Microtubule Dynamics | ||||
Intracellular Trafficking | ||||
Expansion Microscopy | ||||
Cilia Imaging (> 50 fps) | ||||
Single Molecule Live Imaging (not SMLM) e.g. RNA | ||||
Chromatin Remodelling | ||||
Vesicle Trafficking | ||||
Live Membrane Fusion Events | ||||
Cell - Substrate Interaction | ||||
Actin Polymerisation Leading Edge of Cell Motility (TIRF) | ||||
Ultra-Structure of Centrioles (SMLM) | ||||
Nuclear Pore Complexes (SMLM) | ||||
Ultra-Structure of Membranes (SMLM) | ||||
Developmental Biology | ||||
Limb Formation | ||||
Tissue Sample Preparations | ||||
Paraffin Sections | ||||
Whole Organisms up to 500 µm Thick (depends on sample transparency) | ||||
Organoids up to 500 µm Thick (depends on sample transparency) | ||||
Whole Organisms 500+ µm Thick (depends on sample transparency) | ||||
Organoids 500+ µm Thick (depends on sample transparency) | ||||
Intracellular Trafficking | ||||
Gene Expression in Development (with spatial biology) | ||||
Fertilization | ||||
Blood Flow Studies | ||||
Pathogen-Host Interactions (fungus) | ||||
Pathogen-Host Interactions (bacteria) | ||||
Pathogen-Host Interactions (virus) | ||||
Cancer Biology | Large Tissue Slices | |||
Live Imaging Cell Movement & Division | ||||
Organoids up to 500 µm Thick (depends on sample transparency) | ||||
In-Vitro Cell Invasion | ||||
Organoids 500 µm + Thick (depends on sample transparency) | ||||
Gene Expression in Cancer Cells (with spatial biology) | ||||
Cell / Substrate Interaction and Adhesion | ||||
Address Effectiveness of Small Molecule Inhibitors in Cancer Treatment (with TIRF) | ||||
Actin Polymerisation Leading Edge of Cancer Cell Motility (TIRF) | ||||
Ultra-Structure of Centrioles (SMLM) | ||||
Ultra-Structure of Cancer Cell Receptors (SMLM) | ||||
Immunology & Diseases | Fixed Tissues | |||
Large Samples up to 500 µm Thick (depends on sample transparency) | ||||
High Speed Live Imaging up to 40 fps | ||||
Large samples 500+ µm Thick (depends on sample transparency) | ||||
Gene Expression in Disease Cells (with spatial biology) | ||||
High Speed Live Imaging > 40 fps | ||||
Blood Flow | ||||
Cell Surface Infection Dynamics - TIRF | ||||
Mechanisms of Viral Infection | ||||
Microbiology | Intracellular Structure (Super-Resolution SRRF-Stream) | |||
Intracellular Structure (SMLM) (Super - Resolution dSTORM) | ||||
Intracellular Structure (SMLM) (Super - Resolution DNA-PAINT) | ||||
Cell Surface Infection Dynamics - TIRF | ||||
Mechanisms of Viral Infection | ||||
Ultra-Structure of Bacteria Cell Wall (SMLM) | ||||
Ultra-Structure of Virus Capsid Complexes | ||||
Neurobiology | Tissue Sectioning (live and fixed) | |||
Whole Brain Imaging up to 500 µm Thick (depends on sample transparency) | ||||
Whole Brain Imaging 500+ µm Thick | ||||
Map Brain Gene Expression (spatial genomics) | ||||
Calcium Imaging (waves up to 40fps) | ||||
Calcium Imaging (puffs, sparks > 40fps) | ||||
Single Molecule Live Imaging (not SMLM) | ||||
Growth Cone | ||||
Receptor Localisation & Recycling | ||||
Live Vesicular Transport | ||||
Extra Cellular Vesicles Fusion | ||||
Visualise Receptors at the Cell Membrane | ||||
Live cell Imaging of Synaptic Vesicles | ||||
Live Cell Imaging of Neuronal Cell Membrane Fusion | ||||
Resolve Tethered Synaptic Vesicles (SMLM) | ||||
Resolve Synapses in 3D (30 nm axially)(SMLM) | ||||
Biophysics | Protein-Protein Interactions | |||
Protein Membrane Dynamics | ||||
Single Protein Transport | ||||
Endo and Exocytosis | ||||
Localization-Based Super Resolution | ||||
Expansion Microscopy 1,2 | ||||
Multiplex Imaging - Spatially resolved transcriptomics 2,3 | ||||
Multiplex imaging - Spatially resolved proteomics 2,3 |
Notes:
Technique/Technology | BC43 | Dragonfly 200 | Dragonfly 600 | |
Imaging Modes | 2D Imaging | ✔ | ✔ | ✔ |
3D Imaging | ✔ | ✔ | ✔ | |
3D Tile Imaging | ✔ | ✔ | ✔ | |
Deconvolution | ✔ | ✔ | ✔ | |
Multi-well | ✔ | ✔ | ✔ | |
Stitching | ✔ | ✔ | ✔ | |
3D Stitching | ✔ | ✔ | ✔ | |
Finite Burst | ✘ | ✔ | ✔ | |
3D Finite Burst | ✘ | ✔ | ✔ | |
Transmitted Light Microscopy | Differential Phase Contrast (DPC) | ✔ | ✘ | ✘ |
Brightfield | ✔ | ✔ | ✔ | |
Phase Contrast | ✘ | ✔ | ✔ | |
Differential Interference Contrast (DIC) | ✘ | ✔ | ✔ | |
Widefield Imaging | Up to 4 Channels | ✔ | ✔ | ✔ |
More Than 4 Channels | ✘ | ✔ | ✔ | |
Simultaneous Dual Camera Acquisition | ✘ | ✔ | ✔ | |
Confocal Imaging | Single Pinhole Size | ✔ | ✔ | ✔ |
Dual Pinhole Sizes | ✘ | ✔ | ✔ | |
Simultaneous Dual Camera Acquisition | ✘ | ✔ | ✔ | |
Up to 4 Channels | ✔ | ✔ | ✔ | |
More Than 4 Channels | ✘ | ✔ | ✔ | |
Confocal Imaging <500 µm* Thick | ✔ | ✔ | ✔ | |
Confocal Imaging >500 µm* Thick | O | ✔ | ✔ | |
Specialised Microscopy Applications | Compatible with Photostimulation Devices | ✘ | ✔ | ✔ |
TIRF | ✘ | ✘ | ✔ | |
dSTORM | ✘ | ✘ | ✔ | |
3D-STORM | ✘ | ✘ | ✔ | |
DNA-PAINT | ✘ | ✘ | ✔ | |
3D - DNA-PAINT | ✘ | ✘ | ✔ | |
SMLM (Simgle Molecule Localisation Microscopy) | ✘ | ✘ | ✔ | |
Detector Technology | sCMOS | ✔ | ✔ | ✔ |
EMCCD | ✘ | ✔ | ✔ | |
Other Specifications | NIR up to 780nm excitation | ✘ | ✔ | ✔ |
Bench Top Instrument | ✔ | ✘ | ✘ | |
Temperature Control | ✔ | ✔ | ✔ | |
Multi-Position | ✔ | ✔ | ✔ | |
Time Lapse Imaging | ✔ | ✔ | ✔ |
Key: ✔ - Possible, O - Might be Possible, ✘ - Not Possible
* tested on cleared samples