Team:EPF-Lausanne/Notebook/Cloning Strategy

From 2009.igem.org

(Difference between revisions)
(14.07.09)
(Cloning strategy)
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1.Forward primer Trp promoter:
1.Forward primer Trp promoter:
-
 
+
:gtttcttc gaattcgcggccgcttctagagtggcaaatattctgaaatgagctgttgacaattaatcatcgaactagttaactagtacgc
-
gtttcttc gaattcgcggccgcttctagagtggcaaatattctgaaatgagctgttgacaattaatcatcgaactagttaactagtacgc
+
2.Reverse primer Trp promoter:
2.Reverse primer Trp promoter:
-
 
+
:ctagctagctaggtcgataccctttttacgtgaacttgcgtactagttaactagttcgatgattaattgtca
-
ctagctagctaggtcgataccctttttacgtgaacttgcgtactagttaactagttcgatgattaattgtca
+
3.1st Forward primer Inverter TetR:
3.1st Forward primer Inverter TetR:
-
 
+
:aatcatcgaactagttaactagtacgcaagttcacgtaaaaagggtatcgacaaagaggagaaatactagatgtcc
-
aatcatcgaactagttaactagtacgcaagttcacgtaaaaagggtatcgacaaagaggagaaatactagatgtcc
+
4.2nd Forward primer Inverter TetR:
4.2nd Forward primer Inverter TetR:
-
 
+
:gtttcttcgaattcgcggccgcttctagagtggcaaatattctgaaatgagctgttgacaattaatcatcgaactagttaactagta
-
gtttcttcgaattcgcggccgcttctagagtggcaaatattctgaaatgagctgttgacaattaatcatcgaactagttaactagta
+
5.Reverse Primer Inverter TetR:
5.Reverse Primer Inverter TetR:
-
 
+
:ctagctagctag tttctcctctttctctagtagtgc
-
ctagctagctag tttctcctctttctctagtagtgc
+
6.Forward primer ppsR1 R.Palustris CGA009:
6.Forward primer ppsR1 R.Palustris CGA009:
-
 
+
:gtttcttcgaattcgcggccgcttctagatgctggaggatatttgccctggtg
-
gtttcttc*gaattcgcggccgcttctag*atgctggaggatatttgccctggtg
+
7.Reverse primer ppsR1 R.Palustris CGA009:
7.Reverse primer ppsR1 R.Palustris CGA009:
-
 
+
:gtttcttcctgcagcggccgctactagtattactcatcggctccgtctccttc
-
gtttcttc*ctgcagcggccgctactagta*ttactcatcggctccgtctccttc
+
8.Forward primer ppsR2 R.Palustris CGA009:
8.Forward primer ppsR2 R.Palustris CGA009:
-
 
+
:gtttcttcgaattcgcggccgcttctagatggcgtcaaagtccgttcatgcc
-
gtttcttc*gaattcgcggccgcttctag*atggcgtcaaagtccgttcatgcc
+
9.Reverse primer ppsR2 R.Palustris CGA009:
9.Reverse primer ppsR2 R.Palustris CGA009:
-
 
+
:gtttcttcctgcagcggccgctactagtatcaatcctctgcgtcgtctgagg
-
gtttcttc*ctgcagcggccgctactagta*tcaatcctctgcgtcgtctgagg
+
10.Forward primer BrBphP Bradyrhizobium ORS278:
10.Forward primer BrBphP Bradyrhizobium ORS278:
-
 
+
:gtttcttcgaattcgcggccgcttctagatgcccgttccgctgacgac
-
gtttcttc*gaattcgcggccgcttctag*atgcccgttccgctgacgac
+
11.Reverse primer BrBphP Bradyrhizobium ORS278:
11.Reverse primer BrBphP Bradyrhizobium ORS278:
-
 
+
gtttcttcctgcagcggccgctactagtatcactcctcgctctgcgagc
-
gtttcttc*ctgcagcggccgctactagta*tcactcctcgctctgcgagc
+
12.Forward primer ppsR1 Bradyrhizobium ORS278:
12.Forward primer ppsR1 Bradyrhizobium ORS278:
-
 
+
:gtttcttcgaattcgcggccgcttctagatgagggcgttcagagctcc
-
gtttcttc*gaattcgcggccgcttctag*atgagggcgttcagagctcc
+
13.Reverse primer ppsR1 Bradyrhizobium ORS278:
13.Reverse primer ppsR1 Bradyrhizobium ORS278:
-
 
+
:gtttcttcctgcagcggccgctactagtactattccaactgactgtcttcttcgc
-
gtttcttc*ctgcagcggccgctactagta*ctattccaactgactgtcttcttcgc
+
14.Forward primer ppsR2 Bradyrhizobium ORS278:
14.Forward primer ppsR2 Bradyrhizobium ORS278:
-
 
+
:gtttcttcgaattcgcggccgcttctagatggccgagtttcacggtccac
-
gtttcttc*gaattcgcggccgcttctag*atggccgagtttcacggtccac
+
15.Reverse primer ppsR2 Bradyrhizobium ORS278:
15.Reverse primer ppsR2 Bradyrhizobium ORS278:
-
 
+
:gtttcttcctgcagcggccgctactagtactagctccccttttcggtttcctc
-
gtttcttc*ctgcagcggccgctactagta*ctagctccccttttcggtttcctc
+
===15.07.09===
===15.07.09===

Revision as of 15:11, 14 July 2009

Contents


Cloning strategy

July

06.07.09

Four forward primers were designed to amplify:
1.Promoter T7, RBS, CBP and LOVTAP:

gtttcttcgaattcgcggccgcttctagagtaatacgactcactataggggaattgtg

2.RBS, CBP and LOVTAP:

gtttcttcgaattcgcggccgcttctagagtgtttaactttaagaaggag

3.CBP and LOVTAP:

gtttcttcgaattcgcggccgcttctagatgaagcgacgatggaaaaagaatttcatag

4.LOVTAP:

gtttcttcgaattcgcggccgcttctagatgctactacacttgaacgtattgagaagaac

One reverse primer were designed:

gtttcttcctgcagcggccgctactagtatcaatcgcttttcagcaacacctcttc


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

07.07.09

To design plasmids : software Vector NTI

08.07.09

Inducible LOVTAP biobrick strategy

09.07.09

Partial digestion strategy.

10.07.09

13.07.09

Restriction enzymes on [http://www.neb.com/nebecomm/products/category1.asp?#2 Biolabs website] and [http://www.neb.com/nebecomm/tech_reference/restriction_enzymes/cleavage_olignucleotides.asp clevage oligonucleotides]

TRP promoter biobrick strategy

14.07.09

Primers designed for LOVTAP read-out and RBphP project:

1.Forward primer Trp promoter:

gtttcttc gaattcgcggccgcttctagagtggcaaatattctgaaatgagctgttgacaattaatcatcgaactagttaactagtacgc

2.Reverse primer Trp promoter:

ctagctagctaggtcgataccctttttacgtgaacttgcgtactagttaactagttcgatgattaattgtca

3.1st Forward primer Inverter TetR:

aatcatcgaactagttaactagtacgcaagttcacgtaaaaagggtatcgacaaagaggagaaatactagatgtcc

4.2nd Forward primer Inverter TetR:

gtttcttcgaattcgcggccgcttctagagtggcaaatattctgaaatgagctgttgacaattaatcatcgaactagttaactagta

5.Reverse Primer Inverter TetR:

ctagctagctag tttctcctctttctctagtagtgc


6.Forward primer ppsR1 R.Palustris CGA009:

gtttcttcgaattcgcggccgcttctagatgctggaggatatttgccctggtg

7.Reverse primer ppsR1 R.Palustris CGA009:

gtttcttcctgcagcggccgctactagtattactcatcggctccgtctccttc

8.Forward primer ppsR2 R.Palustris CGA009:

gtttcttcgaattcgcggccgcttctagatggcgtcaaagtccgttcatgcc

9.Reverse primer ppsR2 R.Palustris CGA009:

gtttcttcctgcagcggccgctactagtatcaatcctctgcgtcgtctgagg


10.Forward primer BrBphP Bradyrhizobium ORS278:

gtttcttcgaattcgcggccgcttctagatgcccgttccgctgacgac

11.Reverse primer BrBphP Bradyrhizobium ORS278: gtttcttcctgcagcggccgctactagtatcactcctcgctctgcgagc

12.Forward primer ppsR1 Bradyrhizobium ORS278:

gtttcttcgaattcgcggccgcttctagatgagggcgttcagagctcc

13.Reverse primer ppsR1 Bradyrhizobium ORS278:

gtttcttcctgcagcggccgctactagtactattccaactgactgtcttcttcgc

14.Forward primer ppsR2 Bradyrhizobium ORS278:

gtttcttcgaattcgcggccgcttctagatggccgagtttcacggtccac

15.Reverse primer ppsR2 Bradyrhizobium ORS278:

gtttcttcctgcagcggccgctactagtactagctccccttttcggtttcctc

15.07.09

16.07.09

17.07.09

August