Team:ETH Zurich/modeling/xor

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In our design, we are interested in a double flipping. That is to say that two pairs of binding sites surrounds the fragment to be flipped. One pair of binding sites can be bound by DBxb1 and the other one by ΦC31.
In our design, we are interested in a double flipping. That is to say that two pairs of binding sites surrounds the fragment to be flipped. One pair of binding sites can be bound by DBxb1 and the other one by ΦC31.
=== Chemical Species ===
=== Chemical Species ===
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{| class="wikitable"
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|-
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! Name
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! Description
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|-
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|'''mRNA<sub>GFP</sub>'''
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|mRNA for Green fluorescent protein which is produced when the cells are ON.
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|-
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|'''GFP'''
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|Green fluorescent protein which is produced when the cells are ON.
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|-
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|'''mRNA<sub>LuxI</sub>'''
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|mRNA for LuxI which is produced when the cells are ON.
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|-
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|'''LuxI'''
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|Enzyme catalysing the production of LuxAHL from SAM and ACP.
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|-
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|'''mRNA<sub>LasI</sub>'''
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|mRNA for LasI which is produced when the cell are ON.
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|-
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|'''LasI'''
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|Enzyme catalysing  the production of LasAHL from SAM and ACP.
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|}}
=== Reactions ===
=== Reactions ===

Revision as of 11:44, 13 October 2014

iGEM ETH Zurich 2014