Team:Paris/10 August 2009
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===Lab work=== | ===Lab work=== | ||
- | |||
<div class="guillaume"> | <div class="guillaume"> | ||
PCR | PCR | ||
</div> | </div> | ||
<div class="experience"> | <div class="experience"> | ||
- | *For [https://2009.igem.org/Team:Paris/Freezer_PCR_products#A8 A8] and [https://2009.igem.org/Team:Paris/Freezer_PCR_products#A9 A9] | + | *For [https://2009.igem.org/Team:Paris/Freezer_PCR_products#A8 A8] OmpA-Linker and [https://2009.igem.org/Team:Paris/Freezer_PCR_products#A9 A9] pFecA |
+ | *Duplicate with and without DMSO | ||
**1:98°C 1min | **1:98°C 1min | ||
- | **2:98°C 10s | + | **2:98°C 10s |
- | **3:59°C | + | **3:59°C for A8) / 65°C for A9 30s |
**4:72°C 8s | **4:72°C 8s | ||
**5:72°C 10min | **5:72°C 10min | ||
Line 49: | Line 49: | ||
<div class="guillaume"> | <div class="guillaume"> | ||
- | Do | + | Do for sequencing |
</div> | </div> | ||
<div class="experience"> | <div class="experience"> | ||
Line 61: | Line 61: | ||
|width=10%| D0(320) | |width=10%| D0(320) | ||
|width=10%| Dilution Rule | |width=10%| Dilution Rule | ||
+ | |width=10%| Primer Addition | ||
|width=10%| Water Addition | |width=10%| Water Addition | ||
Line 69: | Line 70: | ||
|width=10%| 0.004 | |width=10%| 0.004 | ||
|width=10%| 600/310 = 1.93 ~ 2.0 µL | |width=10%| 600/310 = 1.93 ~ 2.0 µL | ||
- | |width=10%| 2.45 | + | |width=10%| 2.45 µL |
+ | |width=10%| 10.55 µL | ||
|- style="background: #E0E9EF; text-align: center;" | |- style="background: #E0E9EF; text-align: center;" | ||
Line 77: | Line 79: | ||
|width=10%| 0.000 | |width=10%| 0.000 | ||
|width=10%| 600/134 = 4.48 (~ 4.5 µL) | |width=10%| 600/134 = 4.48 (~ 4.5 µL) | ||
- | |width=10%| 2.45 | + | |width=10%| 2.45 µL |
+ | |width=10%| 8.05 µL | ||
|- style="background: #E0E9EF; text-align: center;" | |- style="background: #E0E9EF; text-align: center;" | ||
Line 85: | Line 88: | ||
|width=10%| 0.000 | |width=10%| 0.000 | ||
|width=10%| 600/70 = 8.57 ~ 8.6 µL | |width=10%| 600/70 = 8.57 ~ 8.6 µL | ||
- | |width=10%| 2. | + | |width=10%| 2.45µL |
- | + | |width=10%| 3.95µL | |
|} | |} | ||
- | |||
</div> | </div> | ||
- | <div class=" | + | <div class="guillaume"> |
Gel Migration | Gel Migration | ||
</div> | </div> | ||
<div class="experience"> | <div class="experience"> | ||
+ | GEL!!! | ||
+ | *Remigrate to be sure... pFecA seem to be good but not Ompa-Linker | ||
+ | </div> | ||
- | * | + | <div class="guillaume"> |
+ | Digestion | ||
+ | </div> | ||
+ | <div class="experience"> | ||
+ | *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 | ||
+ | </div> | ||
- | < | + | <div class="guillaume"> |
+ | Purification | ||
+ | </div> | ||
+ | <div class="experience"> | ||
+ | *Promega kit | ||
+ | **50µl final | ||
+ | GEL!!!(strange! none solution fall as quickly in the wholes) | ||
+ | </div> | ||
+ | <div class="guillaume"> | ||
+ | DO<sub>260</sub> | ||
+ | </div> | ||
+ | <div class="experience"> | ||
+ | *D11: RBS-tet : 0,10µg/ml ~730bp | ||
+ | *D12: pSB2K3(pLac) : 0,96µl/ml ~4400bp | ||
+ | </div> | ||
- | * | + | <div class="guillaume"> |
+ | Try for ligation | ||
+ | </div> | ||
+ | <div class="experience"> | ||
+ | *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 H<sub>20</sub> | ||
+ | <br> | ||
+ | *Ligation 1 | ||
+ | **10µl RBS-tetR XbaI/PstI | ||
+ | **1µl pSB2K3(pLac) SpeI/PstI | ||
+ | **2µl Buffer T4 DNA Lygase 10x | ||
+ | **1µl T4 DNA Lygase | ||
+ | **6µl H<sub>20</sub> | ||
+ | <br> | ||
+ | *10min at room temperature (~25?) | ||
+ | *20min at 80°C | ||
+ | </div> | ||
+ | <div class="guillaume"> | ||
+ | Transformation of the ligation | ||
+ | </div> | ||
+ | <div class="experience"> | ||
+ | *As usual, but I forget to done transformation with vector only...so I haven't any control... --! | ||
+ | </div> | ||
- | < | + | <div class="caroline"> |
+ | PCR | ||
</div> | </div> | ||
+ | <div class="experience"> | ||
+ | [https://2009.igem.org/Team:Paris/Freezer_PCR_products#A11 A11] (OmpAsignal) [https://2009.igem.org/Team:Paris/Freezer_PCR_products#A12 A12] (Tg3p) [https://2009.igem.org/Team:Paris/Freezer_PCR_products#A13 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 | ||
+ | |||
+ | Waiting Heigh = A11: 135pb, A12: 274pb, A13: 279pb | ||
+ | |||
+ | ->gel | ||
+ | |||
+ | [[Image:OmpAsignal_fusion_Nterm.JPG]] | ||
+ | |||
+ | |||
+ | [[Image:Tg3p_fusion_N_term.JPG]] | ||
+ | |||
+ | |||
+ | [[Image:TolRII fusion N term.JPG]] | ||
+ | |||
+ | '''A11(OmpAsignal) and A13(TolRII) good and nothing for A12(Tg3p)''' | ||
+ | |||
+ | </div> | ||
<div class="caroline"> | <div class="caroline"> | ||
Purification | Purification | ||
</div> | </div> | ||
<div class="experience"> | <div class="experience"> | ||
- | 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 | + | |
+ | 50µl final | ||
+ | |||
+ | gel purification -> '''Very good''' | ||
+ | |||
+ | [[Image:purif OmpA signal fusion & tolRII fusion N term.JPG]] | ||
+ | |||
+ | Next : Digestion tomorrow | ||
</div> | </div> | ||
<html> | <html> | ||
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|- style="background: #e35050;text-align: center;" | |- style="background: #e35050;text-align: center;" | ||
|Pierre | |Pierre | ||
- | | | + | | modelisation & Algorithmic (a bit...) |
|- style="background: #bababa;text-align: center;" | |- style="background: #bababa;text-align: center;" | ||
|Sylvain | |Sylvain |
Latest revision as of 11:42, 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 | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
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-tetR XbaI/PstI
- 1µl pSB2K3(pLac) SpeI/PstI
- 2µl Buffer T4 DNA Lygase 10x
- 1µl T4 DNA Lygase
- 6µl H20
- 10min at room temperature (~25?)
- 20min at 80°C
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
Waiting Heigh = A11: 135pb, A12: 274pb, A13: 279pb
->gel
A11(OmpAsignal) and A13(TolRII) good and nothing for A12(Tg3p)
Purification
purification on tube n°5 (A11.5 : T°: 70,2 with DMSO and A13.5 : T°73,1 with DMSO)with promega kits
50µl final
gel purification -> Very good
Next : Digestion tomorrow
To do list
Matricule | TODO |
Luc | |
Romain | |
Charlotte | |
Stoff | |
Chris | |
Lisa | |
Caroline | |
Souf | |
Vicard | |
Pierre | modelisation & Algorithmic (a bit...) |
Sylvain | |
Guillaume |