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Team:LMU-Munich/Lab Notebook
From 2011.igem.org
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| - | This week we finally started the most important part of our project: the lab work. So of course we had first of all to setup the lab for our needs. Providing schottbottels, flasks, test glasses, .. | + | This week we finally started the most important part of our project: the lab work. So of course we had first of all to setup the lab for our needs. Providing schottbottels, flasks, test glasses, ... |
| - | + | This week also the first batch of primers arrived so we started the first PCRs. | |
| - | The PCR for prcnA was done using the Phusion polymerase, the primers prcnA-E,N,X-for and prcnA-S-rev. Conditions for the Annealing temperatur were at 50°C. The template was again the gDNA of the E.coli strain MG1655. ([https://2011.igem.org/Team:LMU-Munich/Project/Description For more information about the prcnA-system click here]). | + | The PCR for pnikA was done using the Phusion polymerase, the primers pnikA-E,N,X-for and pnikA-S-rev. The annealing temperature was set for 50°C. The template came from the gDNA of the Escherichia coli strain MG1655. ([https://2011.igem.org/Team:LMU-Munich/Project/Description For more information about the pnikA-system click here]). The expected length of the fragment was 280 bp. |
| + | |||
| + | The PCR for prcnA was done using the Phusion polymerase, the primers prcnA-E,N,X-for and prcnA-S-rev. Conditions for the Annealing temperatur were at 50°C. The template was again the gDNA of the E.coli strain MG1655. ([https://2011.igem.org/Team:LMU-Munich/Project/Description For more information about the prcnA-system click here]). The expected length of the fragment was 230 bp. | ||
| + | |||
| + | The PCRs of pnikA and prcnA were digested with the enzymes EcoRI and SpeI. Together with a reporter they were brought into the backbone pSB1C3 via the Gibson Assembly. The reporters were GFP ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K549001 BBa_K549001]), lacZ' ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K549002 BBa_K549002]] and luxAB ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K549003 BBa_K549003]). | ||
</div> | </div> | ||
Revision as of 12:30, 20 September 2011
Week 1
This week we finally started the most important part of our project: the lab work. So of course we had first of all to setup the lab for our needs. Providing schottbottels, flasks, test glasses, ...
This week also the first batch of primers arrived so we started the first PCRs.
The PCR for pnikA was done using the Phusion polymerase, the primers pnikA-E,N,X-for and pnikA-S-rev. The annealing temperature was set for 50°C. The template came from the gDNA of the Escherichia coli strain MG1655. (For more information about the pnikA-system click here). The expected length of the fragment was 280 bp.
The PCR for prcnA was done using the Phusion polymerase, the primers prcnA-E,N,X-for and prcnA-S-rev. Conditions for the Annealing temperatur were at 50°C. The template was again the gDNA of the E.coli strain MG1655. (For more information about the prcnA-system click here). The expected length of the fragment was 230 bp.
The PCRs of pnikA and prcnA were digested with the enzymes EcoRI and SpeI. Together with a reporter they were brought into the backbone pSB1C3 via the Gibson Assembly. The reporters were GFP ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K549001 BBa_K549001]), lacZ' ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K549002 BBa_K549002]] and luxAB ([http://partsregistry.org/wiki/index.php?title=Part:BBa_K549003 BBa_K549003]).
Week 2
Still doing PCRs and start restriction digests.
Week 3
First Biobrick is ready!
Week 4
Week 5
Week 6
Week 7
Week 8
After weeks of hard work the last week of our lab work started. As we already prepared our BioBricks for sending them last week there was only the shipment left. So on Monday we said Good-bye and hope that they were going to have a nice journey to Boston. So until Wednesday, the Wiki-freeze, are only a few tasks left: finishing the testing of our BioBricks BBa_K549001 and BBa_K549002 and of course to prepare the last thins for the european jamboree in Amsterdam. Making the presentation, the poster and of course ordering our team-sweaters.
Protocols
Primer
pnikA-E,N,X-fwd | GCAGAATTCGCGGCCGCTTCTAGAGTTAAGCCTTGCGATCTGCACC |
pnikA-S-rev | CCGCTACTAGTAGACGATAAAAGACGCACAAGCC |
prcnA-E,N,X-fwd | GCAGAATTCGCGGCCGCTTCTAGAGacggattgtatgagacatggca |
prcnA-S-rev | CCGCTACTAGTAcgcaccaagtaagatggcg |
luxCDrev | CTGCAGCGGCCGCTACTAGTATTAAGACAGAGAAATTGCTTGAT |
PbrR-M,R-fwd | GCAGAATTCGCGGCCGCTTCTAGAGAAGAAGGAGATATACCATGAATATCCAGATCGGCGAG |
PbrR-S,A-rev | AGCCTGCAGCGGCCGCTACTAGTAttaCTAGTCGCTTGGATGGGCG |
pbrRT-S,A-rev | agtcactagtattaaccggttaTTACACCTGGGTAGATGGCC |
pbRMut-fwd | tcgtgcgggattctccagggactgtcggactgc |
pbrMut-rev | tccgacagtccctggagaatcccgcacgattgggc |
ppbrA-E,N,X-fwd | AGCCTGCAGCGGCCGCTACTAGTAGGTTGCGCGTCGCAACGGAAGC |
ppbrA-S-rev | GCAGAATTCGCGGCCGCTTCTAGAGCATGCGGTGCGCTTGGCAAGC |
luxCDfor | GAATTCCGCGGCCGCTTCTAGATGGAAAATGAATCAAAATA |
luxBfor | ATGAAATTTGGATTGTATGAAATTTGGATTGT |
luxBrev | CTGCAGCGGCCGCTACTAGTATTAGGTATATTCC |
luxEfor | GAATTCCGCGGCCGcttctagaATGTGACTGGGGTGAGTGA |
luxErev | CTGCAGCGGCCGCTACTAGTACTATCAAACGCTTCGGTTAA |
iscSfor | AgtcgccggcAAGAAGGAGATATACCATGTACGGAGTTTATAGAGC |
icsSrev | agtcactagtattaaccggtctattaatgatgagcccattcg |
pabAfor | AgtcgccggcAAGAAGGAGATATACCATGAAATTGCTATTAATTGATAATTATG |
pabArev | agtcactagtattaaccggtTTATTACACCACTTTCAAAAAATTATTTAAC |
aurFfor | AgtcgccggcAAGAAGGAGATATACCATGCCACGACACCGCGGGC |
aurFrev | agtcactagtattaaccggttaTCAACGCGGCGTGTGGGGCG |
ChrBAfor | AgtcgccggcAAGAAGGAGATATACCATGAACGCTCTCCCATCCTC |
ChrBArev | agtcactagtattaaccggttaTCAGTGATGCAACAACGGATAGG |
melAfor | gatcTCTAGAtgGCCGGCGCGTGGCTGGTCGGCAAGCCG |
melArev | gatcACCGGTGGCGGACACTATGGCTATTTCTAGC |
