Team:Paris/6 August 2009
From 2009.igem.org
(Difference between revisions)
(→Lab work) |
Christophe.R (Talk | contribs) (→Lab work) |
||
Line 16: | Line 16: | ||
===Lab work=== | ===Lab work=== | ||
- | + | ====Microscope==== | |
- | <div | + | <div class="caroline"> |
FM4-64 dying MG4 and Kayo delete Tol R | FM4-64 dying MG4 and Kayo delete Tol R | ||
- | </div><div | + | </div> |
+ | <div class="experience"> | ||
protocol n°2 (05/08/09) but using PBS | protocol n°2 (05/08/09) but using PBS | ||
Line 28: | Line 29: | ||
->not enough dye | ->not enough dye | ||
</div> | </div> | ||
- | + | ====Molecular Biology==== | |
- | <div | + | <div class="vicard"> |
Gel Migration | Gel Migration | ||
- | </div><div | + | </div> |
+ | <div class="experience"> | ||
*[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 | *[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 | ||
**[[https://2009.igem.org/Team:Paris/Freezer_PCR_products A1]] = Tg3p = 274bp (utiliser le ladder 100bp) | **[[https://2009.igem.org/Team:Paris/Freezer_PCR_products A1]] = Tg3p = 274bp (utiliser le ladder 100bp) | ||
Line 45: | Line 47: | ||
</div> | </div> | ||
- | <div | + | <div class="vicard"> |
Purification and Digestion | Purification and Digestion | ||
- | </div><div | + | </div> |
+ | <div class="experience"> | ||
*Purification of [[https://2009.igem.org/Team:Paris/Freezer_PCR_products A3]], [[https://2009.igem.org/Team:Paris/Freezer_PCR_products A4]]directly in micro-column, [[https://2009.igem.org/Team:Paris/Freezer_PCR_products A5]], [[https://2009.igem.org/Team:Paris/Freezer_PCR_products A6]]directly in micro-column | *Purification of [[https://2009.igem.org/Team:Paris/Freezer_PCR_products A3]], [[https://2009.igem.org/Team:Paris/Freezer_PCR_products A4]]directly in micro-column, [[https://2009.igem.org/Team:Paris/Freezer_PCR_products A5]], [[https://2009.igem.org/Team:Paris/Freezer_PCR_products A6]]directly in micro-column | ||
*Digestion with XbaI and PSTI | *Digestion with XbaI and PSTI |
Revision as of 20:51, 7 August 2009
Contents |
NoteBook
|
|
|
|
|
---|
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
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 | ?? |