Team:Paris/5 August 2009
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|- style="background: #E0E9EF; text-align: center;" | |- style="background: #E0E9EF; text-align: center;" | ||
|width=10%| centri 4000rpm 3min | |width=10%| centri 4000rpm 3min | ||
+ | |width=10%| - | ||
+ | |width=10%| - | ||
|width=10%| - | |width=10%| - | ||
|width=10%| - | |width=10%| - | ||
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|width=10%| + filtrage | |width=10%| + filtrage | ||
|width=10%| + filtrage | |width=10%| + filtrage | ||
+ | |width=10%| - | ||
+ | |width=10%| - | ||
|- style="background: #E0E9EF; text-align: center;" | |- style="background: #E0E9EF; text-align: center;" | ||
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</div> | </div> | ||
<div class="experience"> | <div class="experience"> | ||
- | *[S20] JW4251, [S21] JN0729, [S22] JN0728, [S23] JN0727, [S24] JN0940, | + | *[https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S20 S20] JW4251, [https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S21 S21] JN0729, [https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S22 S22] JN0728, [https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S23 S23] JN0727, [https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S24 S24] JN0940, S24 JN0940, [https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S25 S25] JW5100, S25 JW5100, [https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S26 S26] JN5181, [https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S27 S27] FF64, [https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S28 S28] NEC280. |
</div> | </div> | ||
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</div> | </div> | ||
<div class="experience"> | <div class="experience"> | ||
- | *Purification (using 1%agarose at 30min migration) of | + | *Purification (using 1%agarose at 30min migration) of [https://2009.igem.org/Team:Paris/Freezer_Plasmids#P2 P2]=BBa-J61002 with XbaI PstI (put pTet forward). |
- | *D6=2053pb= | + | *D6=2053pb=[https://2009.igem.org/Team:Paris/Freezer_Plasmids#P2 P2] Digested |
- | * | + | *[https://2009.igem.org/Team:Paris/Freezer_Plasmids#P2 P2]/nothing/ladder 100pb] |
+ | |||
+ | |||
<center>[[Image:GelP2_o.JPG]][[Image:GelP2_coupé_o.JPG]]</center> | <center>[[Image:GelP2_o.JPG]][[Image:GelP2_coupé_o.JPG]]</center> | ||
- | * | + | |
- | * | + | |
+ | *P2 purification checking with 1%agarose at 35 min at 75mV | ||
+ | *P2 | ||
+ | |||
+ | |||
<center>[[Image:Gel_apres_purif_o.JPG]]</center> | <center>[[Image:Gel_apres_purif_o.JPG]]</center> | ||
- | *The purification is ok but | + | |
+ | |||
+ | *The purification is ok but don't use because it's doesn't have pTet, so we have to cut P2 with EcorI and SpeI next time. | ||
</div> | </div> | ||
- | <span/ id=" | + | <span/ id="PCR"> |
<div class="guillaume"> | <div class="guillaume"> | ||
PCR | PCR | ||
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**18µL H<sub>2</sub>0 RNAse/DNAse free (Gibco) | **18µL H<sub>2</sub>0 RNAse/DNAse free (Gibco) | ||
*Dilution DNA 1/10 | *Dilution DNA 1/10 | ||
- | **2µl Genomic DNA of K12 MG1655 ΔrecA::Kan | + | **2µl Genomic DNA of K12 MG1655 ΔrecA::Kan |
**18µL H<sub>2</sub>0 RNAse/DNAse free (Gibco) | **18µL H<sub>2</sub>0 RNAse/DNAse free (Gibco) | ||
*Mix x1 Vf=50µl in PCR tube (in ice) (Add with this order) | *Mix x1 Vf=50µl in PCR tube (in ice) (Add with this order) | ||
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Gel migration | Gel migration | ||
</div> | </div> | ||
- | <div class="experience">*Gel 1%: 5µl of [A1|A2|100bp|A3|A4|1kb|A5|A6] | + | <div class="experience"> |
- | **A1 = Amplification of N-term domain of M13's g3p = 274bp (Useless because we don't use g3p plasmide as matrice => Ctrl-) | + | *Gel 1%: 5µl of [A1|A2|100bp|A3|A4|1kb|A5|A6] |
- | **A2 = Amplification of N-term domain of colicin E3 = 1036bp (Useless because we don't use the right matrice => Ctrl-) | + | **[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A1 A1] = Amplification of N-term domain of M13's g3p = 274bp (Useless because we don't use g3p plasmide as matrice => Ctrl-) |
- | **A3 = Amplification of clyA with RBS in the primer = 987bp | + | **[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A2 A2] = Amplification of N-term domain of colicin E3 = 1036bp (Useless because we don't use the right matrice => Ctrl-) |
- | **A4 = Amplification of OmpA signal for export to periplasm = 135bp | + | **[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A3 A3] = Amplification of clyA with RBS in the primer = 987bp |
- | **A5 = Amplification of tolR = 279bp (Try again because of the second band) | + | **[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A4 A4] = Amplification of OmpA signal for export to periplasm = 135bp |
- | **A6 = Amplification of tatA with RBS = 1634bp (Try again because of the second band) | + | **[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A5 A5] = Amplification of tolR = 279bp (Try again because of the second band) |
+ | **[https://2009.igem.org/Team:Paris/Freezer_PCR_products#A6 A6] = Amplification of tatA with RBS = 1634bp (Try again because of the second band) | ||
+ | |||
+ | |||
<center>[[Image:100bp.png]][[Image:1kb.gif]][[Image:PCR_050809.png]]</center> | <center>[[Image:100bp.png]][[Image:1kb.gif]][[Image:PCR_050809.png]]</center> | ||
</div> | </div> | ||
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</div> | </div> | ||
<div class="experience"> | <div class="experience"> | ||
- | *[S8] DH5α(pSB2K3): LB Kan | + | *[https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S8 S8] DH5α(pSB2K3): LB Kan |
- | *[ | + | *[https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S29 S29] DH5α(pSB1A3): LB Amp |
- | *[ | + | *[https://2009.igem.org/Team:Paris/Freezer_Strains_(Glycerol_stock)#S30 S30] S113 iGEM08 = DH5α(BBa_K136050): LB Amp |
</div> | </div> | ||
<html> | <html> |
Latest revision as of 13:46, 10 August 2009
Contents |
NoteBook
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Lab work
Microscope
FM4-64 dying (wash then stain) strain MG4 | ||||||||||
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n°1 | n°2 | n°3 | n°4 | |||||||
500µl cells | - | - | - | |||||||
centri 4000rpm 3min | - | - | - | |||||||
resuspension 500µl MgSO4 | - | - | - | |||||||
1µl de colorant | 1µl de colorant | 2µl | 2µl | |||||||
incubation 30min 37°C | incubation 60min 37°C | incubation 30min 37°C | incubation 60min 37°C | |||||||
depot sur lame | - | - | - | |||||||
nothing | all cell fluo | so much dye | so much dye |
FM4-64 dying (stain then wash) | ||||||||||
---|---|---|---|---|---|---|---|---|---|---|
n°5 | n°6 | n°9 | n°10 | n°13 | n°14 | |||||
500µl cells | - | - | - | 500µl MgSO4 | 500µl Medium | |||||
1µl de colorant | 1µl de colorant | 1µl | 1µl | 1µl | 1µl | |||||
incubation 30min 37°C | incubation 60min 37°C | incubation 30min 37°C | incubation 60min 37°C | incubation 60min 37°C | incubation 60min 37°C | |||||
centri 4000rpm 3min | - | - | - | - | - | |||||
resuspension 500µl MgSO4 | resuspension 500µl MgSO4 | + filtrage | + filtrage | - | - | |||||
depot sur lame | - | - | - | - | - | |||||
nothing | some cell fluo | noise | noise | noise | noise |
FM4-64 dying with Kayo
protocol like n°2 = all cell fluo, no vesicle
protocol like n°6 = some cell fluo, noise, no vesicle
Molecular biology
Glycerol Stock
Miniprep
- Miniprep for P1/2/3/4/5/7/8
- Same protocol as yesterday. Storage at -20°C.
Purification
- Purification (using 1%agarose at 30min migration) of P2=BBa-J61002 with XbaI PstI (put pTet forward).
- D6=2053pb=P2 Digested
- P2/nothing/ladder 100pb]
- P2 purification checking with 1%agarose at 35 min at 75mV
- P2
- The purification is ok but don't use because it's doesn't have pTet, so we have to cut P2 with EcorI and SpeI next time.
PCR
- Dilution oligo 1/10 (100µM to 10µM)
- 2µl Oligo
- 18µL H20 RNAse/DNAse free (Gibco)
- Dilution DNA 1/10
- 2µl Genomic DNA of K12 MG1655 ΔrecA::Kan
- 18µL H20 RNAse/DNAse free (Gibco)
- Mix x1 Vf=50µl in PCR tube (in ice) (Add with this order)
- 32,5µl H20 RNAse/DNAse free (Gibco)
- 10µl Buffer Polymerase fusion 5x
- 1µl dNTP
- 2,5µl Oligo F 10µM
- 2,5µl Oligo R 10µM
- 1µl Genomic DNA of K12 1/10
- 0,5µl Polymerase Fusion
- Mix x6,5
- 211,25µl H20 RNAse/DNAse free (Gibco)
- 65µl Buffer Polymerase fusion 5x
- 6,5µl dNTP
- 6,5µl Genomic DNA of K12 1/10
- Put 44,5µl of Mix x6,5 in a PCR tube
- Add 2,5µl Oligo F 10µM
- Add 2,5µl Oligo R 10µM
- Add 0,5µl Polymerase Fusion
- For A1/2/3/4/5/6, Program PHUSION:
- 1: 98°C, 1min
- 2: 98°C, 10sec
- 3: 65°C, 30sec
- 4: 72°C, 1min
- Goto 2 29x
- 72°C, 10min
- 4°C, -
Gel migration
- Gel 1%: 5µl of [A1|A2|100bp|A3|A4|1kb|A5|A6]
- A1 = Amplification of N-term domain of M13's g3p = 274bp (Useless because we don't use g3p plasmide as matrice => Ctrl-)
- A2 = Amplification of N-term domain of colicin E3 = 1036bp (Useless because we don't use the right matrice => Ctrl-)
- A3 = Amplification of clyA with RBS in the primer = 987bp
- A4 = Amplification of OmpA signal for export to periplasm = 135bp
- A5 = Amplification of tolR = 279bp (Try again because of the second band)
- A6 = Amplification of tatA with RBS = 1634bp (Try again because of the second band)
ON culture
To do list
Matricule | TODO |
Luc | bacteria coloration microscope protocol |
Romain | Look for his feet |
Charlotte | bibliography on SNAREs/Autotransporters/Jun and Fos complex |
Stoff | merge algo protocol/ Wiki |
Chris | modeling: TeTR |
Lisa | WTF !!! |
Caroline | bacteria coloration microscope protocol |
Souf | if(!oligo){return Wiki;} return PCR; |
Vicard | Lab : Gel / purification / insers |
Pierre | Alice / Tol/Pal modelisation / geophysics |
Sylvain | if(!oligo){return Maltose;} return PCR; |
Guillaume | Miniprep for P(1/2/3/4/5/7/8) / New P7 digestion? / Glycerol Stock (DH5α/Kaio strains) |