Team:Paris/10 August 2009
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*As usual, but I forget to done transformation with vector only...so I haven't any control... --! | *As usual, but I forget to done transformation with vector only...so I haven't any control... --! | ||
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+ | <div class="caroline"> | ||
+ | PCR | ||
+ | </div> | ||
+ | <div class="experience"> | ||
+ | A11(OmpAsignal) A12(Tg3p) A13(TolRII) without (1,2,3) and with DMSO (4,5,6) | ||
+ | |||
+ | temperature gradient | ||
+ | |||
+ | tube n°1/4 : 2/5 : 3/6 | ||
+ | |||
+ | A11 : 68,6 : 70,2 : 71,8 | ||
+ | |||
+ | A12 : 62,2 : 62,9 : 64,0 | ||
+ | |||
+ | A13 : 71,8 : 73,1 : 74,0 | ||
+ | |||
+ | ->gel | ||
+ | |||
+ | A11 and A13 good | ||
+ | |||
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<div class="caroline"> | <div class="caroline"> | ||
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- | purification with promega kits | + | purification on tube n°5 (A11.5 : T°: 70,2 with DMSO and A13.5 : T°73,1 with DMSO)with promega kits |
gel purification -> Very good | gel purification -> Very good | ||
</div> | </div> |
Revision as of 07:59, 11 August 2009
Contents |
NoteBook
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Brain work
edit please ^^
Lab work
PCR
Mini-Prep for Plac
Same Protocol as usual ...
Do for sequencing
Dilution for Plasmids 1,2&3 | ||||||||||
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Plasmid | D0(000) | D0(266/280) | D0(320) | Dilution Rule | Primer Addition | Water Addition | ||||
P1 | 3.10 | 1.72 | 0.004 | 600/310 = 1.93 ~ 2.0 µL | 2.45 µL | 10.55 µL | ||||
P2 | 1.34 | 1.34 | 0.000 | 600/134 = 4.48 (~ 4.5 µL) | 2.45 µL | 8.05 µL | ||||
P3 | 0.70 | 3.39 | 0.000 | 600/70 = 8.57 ~ 8.6 µL | 2.45µL | 3.95µL |
Gel Migration
GEL!!!
- Remigrate to be sure... pFecA seem to be good but not Ompa-Linker
Digestion
- Digestion of P21 (pLac in pSB2K3) with SpeI/PstI (D12) in order to insert D11 RBS-tet (XbaI/PstI)
- 20µl of P21
- Vfinal=50µl
- 2h at 37°C
Purification
- Promega kit
- 50µl final
GEL!!!(strange! none solution fall as quickly in the wholes)
DO260
- D11: RBS-tet : 0,10µg/ml ~730bp
- D12: pSB2K3(pLac) : 0,96µl/ml ~4400bp
Try for ligation
- Ligation between [D12] pSB2K3(pLac) SpeI/PstI and [D11] RBS-tet XbaI/PstI. 20µl final
- Ligation 1
- 4,5µl RBS-tet XbaI/PstI
- 1µl pSB2K3(pLac) SpeI/PstI
- 2µl Buffer T4 DNA Lygase 10x
- 1µl T4 DNA Lygase
- 11,5µl H20
- Ligation 1
- 10µl RBS-tet XbaI/PstI
- 1µl pSB2K3(pLac) SpeI/PstI
- 2µl Buffer T4 DNA Lygase 10x
- 1µl T4 DNA Lygase
- 6µl H20
- 10min at room temperature (~25?)
Transformation of the ligation
- As usual, but I forget to done transformation with vector only...so I haven't any control... --!
PCR
A11(OmpAsignal) A12(Tg3p) A13(TolRII) without (1,2,3) and with DMSO (4,5,6)
temperature gradient
tube n°1/4 : 2/5 : 3/6
A11 : 68,6 : 70,2 : 71,8
A12 : 62,2 : 62,9 : 64,0
A13 : 71,8 : 73,1 : 74,0
->gel
A11 and A13 good
Purification
purification on tube n°5 (A11.5 : T°: 70,2 with DMSO and A13.5 : T°73,1 with DMSO)with promega kits gel purification -> Very good
To do list
Matricule | TODO |
Luc | |
Romain | |
Charlotte | |
Stoff | |
Chris | |
Lisa | |
Caroline | |
Souf | |
Vicard | |
Pierre | modelisation & Algorithmic (a bit...) |
Sylvain | |
Guillaume |