Team:Paris/6 August 2009
From 2009.igem.org
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Gel Migration | Gel Migration | ||
</div><div style="background-color:#E0E9EF; border:1px solid #333333; padding:3px 5px; margin-bottom:10px"> | </div><div style="background-color:#E0E9EF; border:1px solid #333333; padding:3px 5px; margin-bottom:10px"> | ||
- | *[Ladder 1kb|A1|nothing|A2|nothing|A3]using 1% agarose during 30min | + | *[Ladder 1kb|[[https://2009.igem.org/Team:Paris/Freezer_PCR_products A1]]|nothing|[[https://2009.igem.org/Team:Paris/Freezer_PCR_products A2]]|nothing|[[https://2009.igem.org/Team:Paris/Freezer_PCR_products A3]]]using 1% agarose during 30min |
- | **A1 = Tg3p = 274bp (utiliser le ladder 100bp) | + | **[[https://2009.igem.org/Team:Paris/Freezer_PCR_products A1]] = Tg3p = 274bp (utiliser le ladder 100bp) |
- | **A2 = TE3 = 1036bp | + | **[[https://2009.igem.org/Team:Paris/Freezer_PCR_products A2]] = TE3 = 1036bp |
- | ***A1 and A2 didn't work | + | ***[[https://2009.igem.org/Team:Paris/Freezer_PCR_products A1]] and [[https://2009.igem.org/Team:Paris/Freezer_PCR_products A2]] didn't work |
- | **A3 = ClyA (with RBS and poly G linker = 987bp | + | **[[https://2009.igem.org/Team:Paris/Freezer_PCR_products A3]] = ClyA (with RBS and poly G linker = 987bp |
**[for more detail[https://2009.igem.org/Team:Paris/Freezer_PCR_products]] | **[for more detail[https://2009.igem.org/Team:Paris/Freezer_PCR_products]] | ||
<center>[[Image:KR000634.JPG]][[Image:A3coupe.JPG]]</center> | <center>[[Image:KR000634.JPG]][[Image:A3coupe.JPG]]</center> | ||
- | *[Ladder 1kb|nothing|A5|nothing|A5|nothing] using 1% agarose during 30min | + | *[Ladder 1kb|nothing|[[https://2009.igem.org/Team:Paris/Freezer_PCR_products A5]]|nothing|[[https://2009.igem.org/Team:Paris/Freezer_PCR_products A5]]|nothing] using 1% agarose during 30min |
- | **A5=TolRII=279bp[for more detail[https://2009.igem.org/Team:Paris/Freezer_PCR_products]] | + | **[[https://2009.igem.org/Team:Paris/Freezer_PCR_products A5]]=TolRII=279bp[for more detail[https://2009.igem.org/Team:Paris/Freezer_PCR_products]] |
<center>[[Image:KR000637.JPG]][[Image:A5coupé.JPG]]</center> | <center>[[Image:KR000637.JPG]][[Image:A5coupé.JPG]]</center> | ||
</div> | </div> | ||
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Purification and Digestion | Purification and Digestion | ||
</div><div style="background-color:#E0E9EF; border:1px solid #333333; padding:3px 5px; margin-bottom:10px"> | </div><div style="background-color:#E0E9EF; border:1px solid #333333; padding:3px 5px; margin-bottom:10px"> | ||
- | *Purification of A3, A4, A5, A6 | + | *Purification of [[https://2009.igem.org/Team:Paris/Freezer_PCR_products A3]], [[https://2009.igem.org/Team:Paris/Freezer_PCR_products A4]], [[https://2009.igem.org/Team:Paris/Freezer_PCR_products A5]], [[https://2009.igem.org/Team:Paris/Freezer_PCR_products A6]] |
*Digestion with XbaI and PSTI | *Digestion with XbaI and PSTI | ||
</div> | </div> |
Revision as of 14:02, 7 August 2009
NoteBook
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Lab work
FM4-64 dying MG4 and Kayo
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
Gel Migration
Purification and Digestion
Writing tomorow...
- Nouvelles Miniprep pour P1(pSB2K3), P13(pSB1A3), P14(BBa_K136050) => Nulles à refaire pousser ON et miniprep a refaire demain
- ON pour S8(pSB2K3), S29(pSB1A3), S30(BBa_K136050)
- Digestion P1(pSB2K3), P2(BBa_J61002), P7(Bba_R0040) 2h37 par respectivement XP, XS, XP
- Migration sur gel pour verifier 1kb, P1, P2, P7, 100bp
- Transformation 1L7 BBa_J24679 AmpR+ dans DH5a
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 | ?? |