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M1 for Mammalian Cells
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M1 Microfluidic Plate for Mammalian Cells

The M1 plate enables time-lapsed imaging of cultured mammalian cells with solution switching. The microfluidic cell culture region ensures optimal cell health during long term microscopy studies. This design is ideal for switching between up to 6 solutions during imaging, as well as creation of stable spatial gradients. Also see the M16 and M2 microfluidic plate.

 
M1 Plate

Key Features:

• Switch between 6 medium solutions
• Perfusion culture on your microscope for 3+ days
• Ideal for long term spatial gradients
• Pump-free culture in standard incubators
• Pipet friendly sample wells
• #1.5 glass bottom for optimal imaging quality

Ordering Info
Instructions
Technical Note

   

Microfluidic Plate Details
 

M1 Plate Layout

Figure 1. Well Layout

 

The M1 microfluidic plate offers the most advanced technology for live imaging of mammalian cells. Our pioneering microfluidic design allows long term culture of cells on your microscope stage while providing real time solution exchange.

The easy to use format and fool-proof operation allow any user to run long-term live cell imaging experiments with confidence.

The well layout of the M1 plate is schematically depicted in figure 1. There are six flow inlets for solution switching, an open well for imaging, a cell inlet, and a flow outlet.

A #1.5 thickness glass bottom enables high NA imaging on an inverted microscope. The microfluidic plate will fit to any standard 96-well stage holder.

A set of air channels allows gas diffusion into the cell culture area and upstream flow channels (light blue). Due to the high gas permeability of the materials and rapid microscale diffusion, this innovative design maintains a well balanced oxygen or CO2 supply to cultured cells.

The microfluidic cell imaging design is depicted in figure 2. The culture chamber is 1.2x1.2x0.1 mm in size. Cells are introduced via a passive capillary flow method as depicted in figure 3. As cells travel down the streamlines (black arrows), they are loaded into the culture chamber, assuring a low pressure, low stress culture environment.

A key feature of the M1 design is the ability to change the solution exposed to the cells in real time. After switching the flow on the control panel, the solution in the cell culture area will completely turn over as reported in Figure 5. Cells closer to the flow inlets will experience proportionately faster exchange rates.

Flow of 2 or more inlets at the same time will create a spatial gradient across the chamber, enabling cell motility and chemotaxis experiments (figure 8).

The expertly designed microfluidic network ensures rapid laminar flow exchange, continuous flows for over 3 days without refilling, and elimination of cross-flows between the exposure channels.

When imaging is not necessary (e.g. during cell attachment or growth), the plate can be kept in a standard cell culture incubator. A built-in gravity perfusion mechanism allows for many days of continuous medium flow even in the absence of a flow controller. Coupled with the passive cell loading method, pre-culture of cells in the microfluidic plates can be done in your sterile facility without the use of the flow controller. Once the cells are ready, they can be taken from the incubator to your microscope for perfusion experiments.

The small volume of the microfluidic chamber and design of the micro-chamber makes this method especially useful for limited cell samples and primary cells.

Suitable for adherent and non-adherent mammalian cell types. Please contact info@cellasic.com if you have questions regarding a particular cell type.

 

M1 Culture Area

Figure 2. Cell Culture Area

 

M1 Loading

Figure 3. Cell Loading Mechanism

   

M2 Flow
Figure 4. Flow Rate

 
   

M2 Switch Time

Figure 5. Switch Time

 
   

3T3

Figure 6.NIH3T3 cells in the microfluidic device

 
     

hela cell growth

Figure 7 HeLa cell attach and 24hr growth

   

 

   

M1-Gradient

  Figure 8 Spatial gradient in the M1 culture area. Fluorescent dye mixtures are flowed simultaneously from the inlets to create a stable linear gradient.
     
     
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