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Team:ETHZ Basel/Modeling/Interworking
From 2010.igem.org
(Difference between revisions)
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{{ETHZ_Basel10_Modeling}} | {{ETHZ_Basel10_Modeling}} | ||
| - | = Evaluation for | + | = Evaluation for wet laboratory = |
== Goals of the evaluation == | == Goals of the evaluation == | ||
| - | To determine the best possible parts for the biological implementation of E. lemming, combined molecular | + | To determine the best possible parts for the biological implementation of E. lemming, the combined molecular model (Light switch - Chemotaxis) has been used to answer specific questions: |
# Which receptor (Che) protein should be attacked? | # Which receptor (Che) protein should be attacked? | ||
| Line 12: | Line 12: | ||
# In what quantity should the anchor and binding light-sensitive protein be chosen? | # In what quantity should the anchor and binding light-sensitive protein be chosen? | ||
| - | = Evaluation for | + | = Evaluation for information processing = |
| + | == Goal of the evaluation == | ||
| + | Main goal of the evaluation for information processing was to determine time constants of E. lemming by using the combined molecular model (Light switch - Chemotaxis). | ||
Revision as of 07:51, 27 September 2010
Evaluation for wet laboratory
Goals of the evaluation
To determine the best possible parts for the biological implementation of E. lemming, the combined molecular model (Light switch - Chemotaxis) has been used to answer specific questions:
- Which receptor (Che) protein should be attacked?
- To which light-sensitive protein (PhyB, PIF3) should the receptor protein be linked?
- What is a good aspartate concentration?
- In what quantity should the anchor and binding light-sensitive protein be chosen?
Evaluation for information processing
Goal of the evaluation
Main goal of the evaluation for information processing was to determine time constants of E. lemming by using the combined molecular model (Light switch - Chemotaxis).
