Team:ETH Zurich/Process/Microfluidics

From 2011.igem.org

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(Final experimental setup)
(Final experimental setup)
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== '''Final experimental setup''' ==
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== '''Evolution of channel design''' ==
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'''Evolution of channel design'''
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# Microfluidic channel with flow and recycling of the medium
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## Plate with pixel filled with agarose and cell and a microfluidic channel above
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#'''Microfluidic channel with flow and recycling of the medium'''
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## Microfluidic channel with cells sitting in pockets in the channel
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#* Variant 1: Plate with pixel filled with agarose and cell and a microfluidic channel above
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# Microfluidic channel without flow
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#* Variant 2: Microfluidic channel with cells sitting in pockets in the channel
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[[File:ETH_final_setup_sensor.png|600px|center|thumb|'''Experimental setup for SmoColi.''' ]]
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#'''Microfluidic channel without flow'''
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[[File:ETH_final_setup_sensor.png|400px|right|thumb|'''Experimental setup for SmoColi.''' ]]
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:: 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

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Microfluidics
Final Experimental Setup B

Insert text here.

Evolution of channel design

  1. Microfluidic channel with flow and recycling of the medium
    • Variant 1: Plate with pixel filled with agarose and cell and a microfluidic channel above
    • Variant 2: Microfluidic channel with cells sitting in pockets in the channel
  2. Microfluidic channel without flow
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.