Team:ETH Zurich/Process/Microfluidics
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- | == | + | == '''Evolution of channel design''' == |
- | '''Evolution of channel design''' | + | |
- | # Microfluidic channel with flow and recycling of the medium | + | |
- | # | + | #'''Microfluidic channel with flow and recycling of the medium''' |
- | # | + | #* Variant 1: Plate with pixel filled with agarose and cell and a microfluidic channel above |
- | # Microfluidic channel without flow | + | #* Variant 2: Microfluidic channel with cells sitting in pockets in the channel |
- | [[File:ETH_final_setup_sensor.png| | + | #'''Microfluidic channel without flow''' |
+ | [[File:ETH_final_setup_sensor.png|400px|right|thumb|'''Experimental setup for SmoColi.''' ]] | ||
+ | :: The Modeling showed that diffusion and degradation of acetaldehyde/ xylene is enough to create a concentration gradient in the tube. Without a flow there is no need for a liquid so we decided to fill the whole channel with agarose and cells likewise we don´t need recycling because AHL can diffuse through the whole channel. | ||
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Revision as of 20:55, 21 September 2011
Microfluidics |
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Evolution of channel design
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