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- | {{EPF-Lausanne09}}
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- | <div CLASS="epfltrick">__TOC__
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- | </div><div CLASS="epfl09">
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- | =Cloning strategy=
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- | ==July==
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- | ===06.07.09===
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- | Four forward primers were designed to amplify:
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- | <br> 1.Promoter T7, RBS, CBP and LOVTAP:
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- | :gtttcttcgaattcgcggccgcttctagagtaatacgactcactataggggaattgtg
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- | 2.RBS, CBP and LOVTAP:
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- | :gtttcttcgaattcgcggccgcttctagagtgtttaactttaagaaggag
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- | 3.CBP and LOVTAP:
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- | :gtttcttcgaattcgcggccgcttctagatgaagcgacgatggaaaaagaatttcatag
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- | 4.LOVTAP:
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- | :gtttcttcgaattcgcggccgcttctagatgctactacacttgaacgtattgagaagaac
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- | One reverse primer were designed:
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- | :gtttcttcctgcagcggccgctactagtatcaatcgcttttcagcaacacctcttc
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- | The '''recipient IGEM part''' have been chosen: [http://partsregistry.org/partsdb/get_part.cgi?part=BBa_B0010 BBa_B0010], well 13D in the received kit plate 1
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- |
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- | ===07.07.09===
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- | To design plasmids : software Vector NTI
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- |
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- | ===08.07.09===
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- | Inducible LOVTAP biobrick strategy
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- | : Problem to overcome: Pst sites in LOVTAP sequence.
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- | :*Our goal: Biobrick LacI promoter-RBS-LOVTAP-Term ( in this order).
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- | :*Material: Biobrick of LacI promoter, RBS, LOVTAP, Term seperatedly ( LOVTAP obtained from previous section and the rest from iGEM Spring 2009 distribution Kit plate).
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- | :*Strategy: LacI promoter-RBS ligation with iGEM protocol (LacI promoter digested with ES, RBS digested with XP, plasmid containing an other antibiotic digested with EP).
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- | LOVTAP is digested with ES and inserted into Term plasmid (which was digested with EX previously).
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- | Finally, LacI promoter-RBS digested with ES to be inserted into LOVTAP-Term plasmid, digested with EX.
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- |
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- | ===09.07.09===
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- | Partial digestion strategy.
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- | ===10.07.09===
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- |
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- | ===13.07.09===
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- | Restriction enzymes on [http://www.neb.com/nebecomm/products/category1.asp?#2 Biolabs website]
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- | and [http://www.neb.com/nebecomm/tech_reference/restriction_enzymes/cleavage_olignucleotides.asp clevage oligonucleotides]
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- | TRP promoter biobrick strategy
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- | ===14.07.09===
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- | Primers designed for LOVTAP read-out and RBphP project:
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- | 1.Forward primer Trp promoter:
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- | :gtttcttc gaattcgcggccgcttctagagtggcaaatattctgaaatgagctgttgacaattaatcatcgaactagttaactagtacgc
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- | 2.Reverse primer Trp promoter:
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- | :ctagctagctaggtcgataccctttttacgtgaacttgcgtactagttaactagttcgatgattaattgtca
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- | 3.1st Forward primer Inverter TetR:
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- | :aatcatcgaactagttaactagtacgcaagttcacgtaaaaagggtatcgacaaagaggagaaatactagatgtcc
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- | 4.2nd Forward primer Inverter TetR:
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- | :gtttcttcgaattcgcggccgcttctagagtggcaaatattctgaaatgagctgttgacaattaatcatcgaactagttaactagta
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- | 5.Reverse Primer Inverter TetR:
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- | :ctagctagctag tttctcctctttctctagtagtgc
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- | 6.Forward primer ppsR1 R.Palustris CGA009:
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- | :gtttcttcgaattcgcggccgcttctagatgctggaggatatttgccctggtg
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- | 7.Reverse primer ppsR1 R.Palustris CGA009:
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- | :gtttcttcctgcagcggccgctactagtattactcatcggctccgtctccttc
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- | 8.Forward primer ppsR2 R.Palustris CGA009:
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- | :gtttcttcgaattcgcggccgcttctagatggcgtcaaagtccgttcatgcc
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- | 9.Reverse primer ppsR2 R.Palustris CGA009:
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- | :gtttcttcctgcagcggccgctactagtatcaatcctctgcgtcgtctgagg
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- | 10.Forward primer BrBphP Bradyrhizobium ORS278:
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- | :gtttcttcgaattcgcggccgcttctagatgcccgttccgctgacgac
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- | 11.Reverse primer BrBphP Bradyrhizobium ORS278:
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- | :gtttcttcctgcagcggccgctactagtatcactcctcgctctgcgagc
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- | 12.Forward primer ppsR1 Bradyrhizobium ORS278:
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- | :gtttcttcgaattcgcggccgcttctagatgagggcgttcagagctcc
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- | 13.Reverse primer ppsR1 Bradyrhizobium ORS278:
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- | :gtttcttcctgcagcggccgctactagtactattccaactgactgtcttcttcgc
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- | 14.Forward primer ppsR2 Bradyrhizobium ORS278:
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- | :gtttcttcgaattcgcggccgcttctagatggccgagtttcacggtccac
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- | 15.Reverse primer ppsR2 Bradyrhizobium ORS278:
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- | :gtttcttcctgcagcggccgctactagtactagctccccttttcggtttcctc
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- | ===15.07.09===
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- |
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- | ===16.07.09===
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- |
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- | ===17.07.09===
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- |
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- | ==August==
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- |
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- | </div><div CLASS="epfl09bouchon"></div>
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