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Team:Paris Saclay/Notebook/July/16
From 2013.igem.org
(Difference between revisions)
| Line 7: | Line 7: | ||
==='''A - Aerobic/Anaerobic regulation system'''=== | ==='''A - Aerobic/Anaerobic regulation system'''=== | ||
| - | ===='''Objective : obtaining | + | ===='''Objective : obtaining BBa_K1155003, BBa_K1155007'''==== |
| - | ===='''1 - Extraction of | + | ===='''1 - Extraction of BBa_B0015, BBa_B0017, BBa_I732019 from DH5α'''==== |
Zhou | Zhou | ||
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Protocol : [[Team:Paris_Saclay/extraction|High copy plamid extraction]] | Protocol : [[Team:Paris_Saclay/extraction|High copy plamid extraction]] | ||
| - | ===='''2 - Digestion of | + | ===='''2 - Digestion of BBa_B0015, BBa_B0017, BBa_I732019 by EcoRI/PstI'''==== |
Anaïs | Anaïs | ||
| Line 74: | Line 74: | ||
==='''B - PCB sensor system'''=== | ==='''B - PCB sensor system'''=== | ||
| - | ===='''Objective : obtaining | + | ===='''Objective : obtaining BBa_K1155001, BBa_K1155002, BphR2 in PSB1C3'''==== |
| - | ===='''1 - Electrophoresis of the digestion of | + | ===='''1 - Electrophoresis of the digestion of BBa_K1155001, BBa_K1155002, BphR2 in PSB1C3'''==== |
Anaïs, Zhou | Anaïs, Zhou | ||
| - | * | + | * BBa_K1155001 : |
{| | {| | ||
| style="width:350px;border:1px solid black;" |[[File:Psgel21607.jpg|300px]] | | style="width:350px;border:1px solid black;" |[[File:Psgel21607.jpg|300px]] | ||
| style="width:350px;border:1px solid black;vertical-align:top;" | | | style="width:350px;border:1px solid black;vertical-align:top;" | | ||
| - | * Well 1 to 5 : 2µL | + | * Well 1 to 5 : 2µL BBa_K1155001 digested by EcoRI/PstI+2µl of 6X loading dye |
| - | * Well 6 and 7 : 2µL | + | * Well 6 and 7 : 2µL BBa_K1155001 digested by SacII+2µl of 6X loading dye |
* Well 8 : 6µL DNA Ladder | * Well 8 : 6µL DNA Ladder | ||
* Gel : 1.2% | * Gel : 1.2% | ||
| Line 92: | Line 92: | ||
Expected size : | Expected size : | ||
| - | * | + | * BBa_K1155001 digested by EcoRI/PstI : 2037bp + 333bp |
| - | * | + | * BBa_K1155001 digested by SacII : 2370bp |
{| | {| | ||
| style="border:1px solid black;padding:5px;background-color:#DEDEDE;" | | | style="border:1px solid black;padding:5px;background-color:#DEDEDE;" | | ||
| - | We obtain fragment at the right size. We will amplify | + | We obtain fragment at the right size. We will amplify BBa_K1155001. |
|} | |} | ||
| - | * | + | * BBa_K1155002 : |
{| | {| | ||
| style="width:350px;border:1px solid black;" |[[File:Psgel31607.jpg|500px]] | | style="width:350px;border:1px solid black;" |[[File:Psgel31607.jpg|500px]] | ||
| style="width:350px;border:1px solid black;vertical-align:top;" | | | style="width:350px;border:1px solid black;vertical-align:top;" | | ||
| - | * Well 1 to 8 : 2µL | + | * Well 1 to 8 : 2µL BBa_K1155002 digested by EcoRI/PstI+2µl of 6X loading dye |
* Well 9 : 6µL DNA Ladder | * Well 9 : 6µL DNA Ladder | ||
| - | * Well 10 to 17 : 2µL | + | * Well 10 to 17 : 2µL BBa_K1155002 digested by SacII+2µl of 6X loading dye |
* Gel : 1.5% | * Gel : 1.5% | ||
|} | |} | ||
Expected size : | Expected size : | ||
| - | * | + | * BBa_K1155002 digested by EcoRI/PstI : ... |
| - | * | + | * BBa_K1155002 digested by SacII : ... |
{| | {| | ||
Revision as of 09:51, 30 September 2013
Notebook : July 16
Lab work
A - Aerobic/Anaerobic regulation system
Objective : obtaining BBa_K1155003, BBa_K1155007
1 - Extraction of BBa_B0015, BBa_B0017, BBa_I732019 from DH5α
Zhou
Protocol : High copy plamid extraction
2 - Digestion of BBa_B0015, BBa_B0017, BBa_I732019 by EcoRI/PstI
Anaïs
- DNA : 5µL
- Buffer FD : 2µL
- EcoRI FD : 1µL
- PstI FD : 1µL
- H2O : 21µL
We let our digestion 1h30 at 37°C.
Objective : obtaining biobricks in PSB3K3
1 - Digestion of PSB3K3 by EcoRI/PstI
Anaïs
Used quantities :
- DNA : 5µL
- Buffer FD : 2µL
- EcoRI FD : 1µL
- PstI FD : 1µL
- H2O : 11µL
We let our digestion 1h30 at 37°C.
2 - Electrophoresis of the digestion of PSB3K3 by EcoRI/PstI
Sheng
|
|
Expected sizes :
- PSB3K3 : 2750bp
|
We obtain fragments at the right size. |
3 - Gel purification of electrophoresis of the digestion of PSB3K3 by EcoRI/PstI
Abdou
Protocol : [http://www.mn-net.com/tabid/1452/default.aspx Gel purification ]
B - PCB sensor system
Objective : obtaining BBa_K1155001, BBa_K1155002, BphR2 in PSB1C3
1 - Electrophoresis of the digestion of BBa_K1155001, BBa_K1155002, BphR2 in PSB1C3
Anaïs, Zhou
- BBa_K1155001 :
|
|
Expected size :
- BBa_K1155001 digested by EcoRI/PstI : 2037bp + 333bp
- BBa_K1155001 digested by SacII : 2370bp
|
We obtain fragment at the right size. We will amplify BBa_K1155001. |
- BBa_K1155002 :
|
|
Expected size :
- BBa_K1155002 digested by EcoRI/PstI : ...
- BBa_K1155002 digested by SacII : ...
|
We didn't obtain fragments at the right size. We will do the ligation again. |
- BphR2 in PSB1C3 :
|
|
Expected size :
- BphR2 digested by EcoRI/PstI : ...
- BphR2 digested by SacII : ...
|
We didn't obtain fragments at the right size. After reading the sequence again, we find an digestion site in the middle of our biobrick. We will do a Gibson assembly to modify this site. |
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