"
LOVTAP
From 2009.igem.org
(→To do) |
(→To do) |
||
| Line 9: | Line 9: | ||
<br> Purification protocol | <br> Purification protocol | ||
<br> Digest assay protocol | <br> Digest assay protocol | ||
| - | <br><span style="color:grey">Idea of letter :[[Media:letter_strickland.pdf]] | + | <br><span style="color:grey">Idea of letter :[[Media:letter_strickland.pdf]] |
;- Biobricks | ;- Biobricks | ||
Revision as of 21:19, 1 June 2009
To find
- Sequence of the 12 mutant fusion proteins or LOV domain AND TrpR (separately) => PUBMED (http://www.ncbi.nlm.nih.gov/)
To do
- - Find the exact genetic circuit for Trp repressor Nath
- - Write an e-mail to Strickland et al to ask Basile first shot; I think we could then look at it all together
Sequence (of all 12 fusion proteins)
Purification protocol
Digest assay protocol
Idea of letter :Media:letter_strickland.pdf
- - Biobricks
Look for a (or many) paper(s) that characterizes E.Coli Trp repressor, and find the Trp operon sequence Mél
Summary of what characterizes E.Coli Trp repressor : Media:The_tryptophan_biosynthetic_pathway.pdf
One good article : RNA-based_regulation_of_genes_of_tryptophan_synthesis_an_degradation.pdf
Sequence from NCBI : Media:Sequence_du_Trp_repressor.txt
Design a biobrick that coexpresses LOVTAP and mCherry (after Trp operon) when LOVTAP bind the Trp operon. Design a switch on/off read out.
| Home | The Team | The Project | Parts Submitted to the Registry | Modeling | Notebook | Lectures | Team Management |
|---|
