Team:Paris Saclay/Notebook/August/5
From 2013.igem.org
(→3 - Electrophoresis of PCR of pSB1C3) |
(→1 - Colony PCR of BBa_K1155004, BBa_K115005, BBa_K1155006 in DH5α) |
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===='''Objective : obtaining BBa_K1155004, BBa_K1155005, BBa_K1155006'''==== | ===='''Objective : obtaining BBa_K1155004, BBa_K1155005, BBa_K1155006'''==== | ||
- | ===='''1 - | + | ===='''1 - PCR Colonies of BBa_K1155004, BBa_K115005, BBa_K1155006 in DH5α'''==== |
Damir, Nadia, XiaoJing | Damir, Nadia, XiaoJing | ||
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- | We | + | We took a single colony and resuspend in 10µL H2O. |
Used quantities : | Used quantities : | ||
- | * DNA : 2µL | + | * DNA : 2µL H2O of resuspend colony |
* Mix : (it was divided in 25 tubes for 25 different colonies for each promotor with 23µL of mix in each tube) | * Mix : (it was divided in 25 tubes for 25 different colonies for each promotor with 23µL of mix in each tube) | ||
** Oligo 44 : 3.5µL | ** Oligo 44 : 3.5µL |
Revision as of 17:58, 3 October 2013
Notebook : August 5
Lab work
A - Aerobic/Anaerobic regulation system
Objective : obtaining BBa_K1155003
1 - Digestion of BBa_K1155003 by EcoRI/PstI to check the ligation between RBS-Amil CP,Term and pSB1C3
Nadia, XiaoJing
Used quantities :
- BBa_K1155003 : 5µL
- EcoRI FD : 1µL
- PstI FD : 1µL
- Buffer FD : 3µL
- H2O : 20µL
We incubate the digestion at 37°C during 15 minutes.
2 - Electrophoresis of the digestion of BBa_K1155003
Damir
Expected sizes :
- RBS_AmilCP-Term : 824bp
- pSB1C3 : 2070bp
We obtain fragments at the right size. We will sequence it. |
Objective : obtaining BBa_K1155007
1 - Digestion of BBa_I732017 by EcoRI/SpeI
Abdou, Damir, Nadia,
Used quantities :
- BBa_I732017 : 41µL
- Buffer FD : 5µL
- EcoRI : 2µL
- SpeI : 2µL
We incubate the digestion at 37°C for 1h30.
2 -Electrophoresis of the digestion of BBa_I732017 by EcoRI/SpeI
Damir, Nadia
|
Expected sizes :
- RBS-LacZ : 3093 bp
- pSB1A2 : 2079 bp
We obtain fragments at the right size. We will make an electro-elution to extract RBS-LacZ. |
3 - PCR of pSB1C3
Nadia, XiaoJing
Used quantities :
- pSB1C3 : 2µL
- Buffer phusion : 10µL
- Oligo 64 : 2.5µL
- Oligo 65 : 2.5µL
- dNTP : 1µL
- enzyme Phusion : 0.25µL
- H2O : 36.75µL
PCR program :
Hybridation temperature gradient :
A - 65°C/ B - 64.7°C/ C - 64.1°C/ D - 63.1°C/ E - 62°C/ F - 61.2°C/ G - 60.5°C/ H - 60°C/
3 - Electrophoresis of PCR of pSB1C3
Nadia, XiaoJing
|
Expected sizes :
- pSB1C3 : 2070bp
We obtain fragments at the right size. We will purify it. |
4 - Gel purification of electrophoresis of PCR of pSB1C3
Nadia, XiaoJing
Protocol : [http://www.mn-net.com/tabid/1452/default.aspx Gel purification ]
Objective : obtaining BBa_K1155004, BBa_K1155005, BBa_K1155006
1 - PCR Colonies of BBa_K1155004, BBa_K115005, BBa_K1155006 in DH5α
Damir, Nadia, XiaoJing
Transformation of 07/31/13 works. We will do a PCR Colony. |
We took a single colony and resuspend in 10µL H2O.
Used quantities :
- DNA : 2µL H2O of resuspend colony
- Mix : (it was divided in 25 tubes for 25 different colonies for each promotor with 23µL of mix in each tube)
- Oligo 44 : 3.5µL
- Oligo 45 : 3.5µL
- Buffer Dream Taq : 70µL
- dNTP : 28µL
- Dream Taq : 5µL
- H2O : 590µL
PCR Program :
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