Temperature control devices comparative

Use CherryTemp™ microfluidic technology for fast and accurate temperature switch during microscope observation.

⇒ Choose the adequate system for your cells

CherryTemp Temperature control for microscopy

The technology relies on a sophisticated, electronically controlled microfluidics loop associated with ultra-fast heater-cooler exchangers system.

Δ Temperature: 5 to 45C

Pros: ultra-fast temperature shift (5 to 45 C in seconds), temperature stability (±0,1C), dual-temperature pre-set up for fast temperature switch, immersion objective and DIC illumination heat loss integrated correction, sub-cellular high-resolution imaging, no cell stress

Cons: not adequate for long-run experiments

Heated microscope stage

Microscope stage temperature is controlled using Peltier or liquid based heated platform. Temperature controlled microscope stages modify the temperature of the biological sample by thermal diffusion through the glass slide or metal heat conducting bridge to minimize the temperature gradient over the sample.

ΔTemperature: -196°C to 100°C (for the best set-up)

Pros: high temperature range, fast temperature switch (2-3 min), easy to use

Cons: poor temperature uniformity, only one temperature can be pre-set, additional temperature control for immersion objective required, single area temperature control, heat-diffusion to nearby microscope equipment

Incubation chamber

This type of devices provides a multi-parameters (gas, pH and temperature) controlled environment within a plexiglas box.

Δ Temperature: 15 to 60C

Pros: easy to use, homogenous temperature, fits Petri dishes, long run experiments

Cons: slow temperature switch,  temperature loss during long DIC illumination or immersion objective, mono-temperature applied on sample, cumbersome if intervention is needed on the sample


In this system, the dish is directly perfused with a pre-heated fluid. This system is adapted for experiments requiring rapid temperature shift with medium renewal

ΔTemperature : ambient to 50C

Pros: fast temperature switch (less than a minute), homogenous temperature, objective-induced heat loss is controlled by warm fluid, medium renewal

Cons: cell stress due to shear fluid flow forces, flushing of chemical molecules due to fluid flow, fluid movement affects focal plane, mono-temperature applied on sample

Objective heater

They are used as a complement to perfusion systems or thermalized stage in order to minimize the immersion objective thermal gradient. There exists electronic heater collars and fluidic collars.

ΔTemperature: ambient to 43C, if thermalized+pumping system 0 to 100C

Pros: enhance temperature uniformity of pre-existing temperature controller devices, large temperature range

Cons: in complement with other temperature controller, slow temperature shift, difficult of use

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