Team:Paris/6 August 2009
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==NoteBook== | ==NoteBook== | ||
- | { | + | {{Paris2009_Calendar}} |
- | + | {{Paris2009_Calendar_Link|5_August_2009|7_August_2009}} | |
- | + | <center> '''August 6th''' </center> | |
- | + | ||
- | + | ||
- | + | ||
- | + | ||
<html> | <html> | ||
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</html> | </html> | ||
+ | ===Lab work=== | ||
+ | ====Microscope==== | ||
+ | <div class="caroline"> | ||
+ | FM4-64 dying MG4 and Kayo delete Tol R | ||
+ | </div> | ||
+ | <div class="experience"> | ||
+ | protocol n°2 (05/08/09) but using PBS | ||
- | + | ->nearly the same as MgSO4 | |
+ | protocol n°2 (05/08/09)but 1ml of cells and 1µl of dye, one with MgSO4 and one with PBS | ||
- | + | ->not enough dye | |
- | + | ||
- | + | ||
- | + | ||
</div> | </div> | ||
- | <div | + | ====Molecular Biology==== |
+ | <div class="vicard"> | ||
+ | Gel Migration | ||
</div> | </div> | ||
- | <div | + | <div class="experience"> |
- | + | *[Ladder 1kb|[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A1 A1]|nothing|[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A2 A2]|nothing|[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A3 A3]]using 1% agarose during 30min | |
+ | **[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A1 A1] = Tg3p = 274bp (utiliser le ladder 100bp) | ||
+ | **[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A2 A2] = TE3 = 1036bp | ||
+ | **[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A3 A3] = ClyA (with RBS and poly G linker = 987bp | ||
- | + | <center>[[Image:KR000634.JPG]][[Image:A3_cut.JPG]]</center> | |
- | |||
+ | *[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A1 A1] and [https://2009.igem.org/Team:Paris/Freezer_PCR_products#A2 A2] didn't work we don't see it on the gel because it's not in E.Coli. | ||
+ | *[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A3 A3] didn't migrate very well | ||
+ | **[Ladder 1kb|nothing|[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A5 A5]|nothing|[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A5 A5]|nothing] using 1% agarose during 30min | ||
+ | **[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A5 A5] = TolRII = 279bp | ||
+ | |||
+ | <center>[[Image:KR000637.JPG]][[Image:A5_coupe.JPG]]</center> | ||
+ | </div> | ||
+ | |||
+ | <div class="vicard"> | ||
+ | Purification and Digestion | ||
+ | </div> | ||
+ | <div class="experience"> | ||
+ | *Purification of [https://2009.igem.org/Team:Paris/Freezer_PCR_products#A3 A3], [https://2009.igem.org/Team:Paris/Freezer_PCR_products#A4 A4] directly in micro-column, [https://2009.igem.org/Team:Paris/Freezer_PCR_products#A5 A5], [https://2009.igem.org/Team:Paris/Freezer_PCR_products#A6 A6] using gel then micro-column | ||
+ | *Digestion with XbaI and PSTI | ||
+ | </div> | ||
+ | |||
+ | <div class="guillaume"> | ||
+ | New Miniprep | ||
+ | </div> | ||
+ | <div class="experience"> | ||
+ | *New Miniprep for [https://2009.igem.org/Team:Paris/Freezer_Plasmids#P1 P1]: pSB2K3, [https://2009.igem.org/Team:Paris/Freezer_Plasmids#P13 P13]: pSB1A3, [https://2009.igem.org/Team:Paris/Freezer_Plasmids#P14 P14]: BBa_K136050 (RBS tetR) | ||
+ | *Result: Just good for trash. Make new ON culture. | ||
+ | </div> | ||
+ | <div class="guillaume"> | ||
+ | Digestion by XbaI/PstI (XP) or XbaI/SpeI (XS) | ||
+ | </div> | ||
+ | <div class="experience"> | ||
+ | *[https://2009.igem.org/Team:Paris/Freezer_Plasmids#P1 P1]: pSB2K3 by XP | ||
+ | *[https://2009.igem.org/Team:Paris/Freezer_Plasmids#P2 P2]: BBa_J61002 (plasmid backbone with RFP) by XS | ||
+ | *[https://2009.igem.org/Team:Paris/Freezer_Plasmids#P7 P7]: Bba_R0040 (ptet) by XP | ||
+ | Digestion during 2h at 37°C. | ||
+ | </div> | ||
+ | <div class="guillaume"> | ||
+ | Gel migration | ||
+ | </div> | ||
+ | <div class="experience"> | ||
+ | *Gel migration for [https://2009.igem.org/Team:Paris/Freezer_Plasmids#P1 P1]: pSB2K3, [https://2009.igem.org/Team:Paris/Freezer_Plasmids#P2 P2]: BBa_J61002 (plasmid backbone with RFP), [https://2009.igem.org/Team:Paris/Freezer_Plasmids#P7 P7]: BBa_R0040 (ptet) | ||
+ | *[1kb|P1|P2|P7|100bp|/] | ||
+ | |||
+ | <center>[[Image:Wikidigestion060809.png]]</center> | ||
+ | |||
+ | *Result: | ||
+ | **pSB2K3: wrong bande. Try again... | ||
+ | **plasmid backbone with RFP: Wrong enzymes?! | ||
+ | **ptet: good but the 1500bp band must not be there! | ||
+ | </div> | ||
+ | <div class="guillaume"> | ||
+ | ON culture | ||
+ | </div> | ||
+ | <div class="experience"> | ||
+ | *ON culture for [https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S8 S8]: pSB2K3, [https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S29 S29]: pSB1A3, [https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S30 S30]: BBa_K136050 (RBS tetR) in order to done new miniprep | ||
+ | </div> | ||
+ | <div class="guillaume"> | ||
+ | Transformation | ||
+ | </div> | ||
+ | <div class="experience"> | ||
+ | *Resuspention of biobrick BBa_J2479 (1L7) | ||
+ | *Transformation in competent DH5α | ||
+ | </div> | ||
<html> | <html> | ||
</div> | </div> | ||
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</html> | </html> | ||
+ | ===To do list=== | ||
+ | {| | ||
+ | |- style="background: #ccccff; text-align: center;" | ||
+ | |width=100px| Matricule | ||
+ | |width=800px| TODO | ||
+ | |- style="background: #59eb26;text-align: center;" | ||
+ | |Luc | ||
+ | |Labs | ||
+ | |- style="background: #efe715;text-align: center;" | ||
+ | |Romain | ||
+ | |Look for his feet | ||
+ | |- style="background: #d8279c;text-align: center;" | ||
+ | |Charlotte | ||
+ | |Jun/Fos system (oligo + system) | ||
+ | |- style="background: #fbfbfb;text-align: center;" | ||
+ | |Stoff | ||
+ | |DataBase / kitchen system ? | ||
+ | |- style="background: #0824f5;text-align: center;" | ||
+ | |Chris | ||
+ | |modeling: model genetique network / next week lab planning / gillepsy | ||
+ | |- style="background: #06ff00;text-align: center;" | ||
+ | |Lisa | ||
+ | |WTF !!! | ||
+ | |- style="background: #b40ecd;text-align: center;" | ||
+ | |Caroline | ||
+ | |lab / microscope | ||
+ | |- style="background: #ff9966;text-align: center;" | ||
+ | |Souf | ||
+ | |lab / oligo / wiki | ||
+ | |- style="background: #79f4f8;text-align: center;" | ||
+ | |Vicard | ||
+ | |Lab : Gel :D | ||
+ | |- style="background: #e35050;text-align: center;" | ||
+ | |Pierre | ||
+ | |Tol/pal modeling | ||
+ | |- style="background: #bababa;text-align: center;" | ||
+ | |Sylvain | ||
+ | |if(!oligo){return Maltose;} return PCR; | ||
+ | |- style="background:green; text-align: center;" | ||
+ | |Guillaume | ||
+ | |Lab | ||
+ | |} | ||
- | |||
- | + | {{Paris2009_Calendar_Link|5_August_2009|7_August_2009}} |
Latest revision as of 09:22, 13 August 2009
Contents |
NoteBook
|
|
|
|
|
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Lab work
Microscope
FM4-64 dying MG4 and Kayo delete Tol R
protocol n°2 (05/08/09) but using PBS
->nearly the same as MgSO4
protocol n°2 (05/08/09)but 1ml of cells and 1µl of dye, one with MgSO4 and one with PBS
->not enough dye
Molecular Biology
Gel Migration
- A1 and A2 didn't work we don't see it on the gel because it's not in E.Coli.
- A3 didn't migrate very well
Purification and Digestion
New Miniprep
Digestion by XbaI/PstI (XP) or XbaI/SpeI (XS)
Digestion during 2h at 37°C.
Gel migration
- Gel migration for P1: pSB2K3, P2: BBa_J61002 (plasmid backbone with RFP), P7: BBa_R0040 (ptet)
- [1kb|P1|P2|P7|100bp|/]
- Result:
- pSB2K3: wrong bande. Try again...
- plasmid backbone with RFP: Wrong enzymes?!
- ptet: good but the 1500bp band must not be there!
ON culture
Transformation
- Resuspention of biobrick BBa_J2479 (1L7)
- Transformation in competent DH5α
To do list
Matricule | TODO |
Luc | Labs |
Romain | Look for his feet |
Charlotte | Jun/Fos system (oligo + system) |
Stoff | DataBase / kitchen system ? |
Chris | modeling: model genetique network / next week lab planning / gillepsy |
Lisa | WTF !!! |
Caroline | lab / microscope |
Souf | lab / oligo / wiki |
Vicard | Lab : Gel :D |
Pierre | Tol/pal modeling |
Sylvain | if(!oligo){return Maltose;} return PCR; |
Guillaume | Lab |