Team:Evry/auxin detection

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<h2> Overview </h2>
<h2> Overview </h2>
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Now that we’ve managed to model auxin creation and transport, you may be asking yourself ; great, those guys have done all those models, but how can we link it to what we see ?
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That’s the aim of this model that will link the quantity of auxin transported into the cell to GFP degradation that we can observe in our tadpole’s cells.
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As for us, this model will also help our biologists to find the conditions upon which the reception can work and the help them guess the reasons of possible dysfunction in the auxin reception.
<h2> Hypotheses </h2>
<h2> Hypotheses </h2>
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The same promoter is used for the creation of GFP and TIR, so the efficiency  Gamma for the creation of GFP and TIR1 will be identical.
<h2> Descritpion of the model </h2>
<h2> Descritpion of the model </h2>
<h2> Model's calibration </h2>
<h2> Model's calibration </h2>

Revision as of 11:33, 18 September 2012

Auxin detection

Overview

Now that we’ve managed to model auxin creation and transport, you may be asking yourself ; great, those guys have done all those models, but how can we link it to what we see ? That’s the aim of this model that will link the quantity of auxin transported into the cell to GFP degradation that we can observe in our tadpole’s cells. As for us, this model will also help our biologists to find the conditions upon which the reception can work and the help them guess the reasons of possible dysfunction in the auxin reception.

Hypotheses

The same promoter is used for the creation of GFP and TIR, so the efficiency Gamma for the creation of GFP and TIR1 will be identical.

Descritpion of the model

Model's calibration

Results

Criticisms

Confrontation with exepriences

Conclusion

References