Team:Paris Saclay/Notebook/August/6
From 2014.igem.org
(Difference between revisions)
(→PCR Cleanup) |
(→C - Salicylate Inducible Suppressing System) |
||
Line 3: | Line 3: | ||
==Lab work== | ==Lab work== | ||
===C - Salicylate Inducible Suppressing System=== | ===C - Salicylate Inducible Suppressing System=== | ||
+ | ====Plasmid DNA Purification==== | ||
+ | ''by Eugene and Fabio'' | ||
+ | * BBa_K1372000 Cl.1 | ||
+ | * BBa_K1372000 Cl.2 | ||
+ | From Liquid Culture made the [https://2014.igem.org/Team:Paris_Saclay/Notebook/August/5#C_-_Salicylate_Inducible_Suppressing_System 5th August] | ||
+ | |||
+ | [https://2014.igem.org/Team:Paris_Saclay/Protocols/Extraction_of_the_Genomic_DNA_from_Bacteria_by_using_NucleoSpin®_Tissue Protocol] | ||
====Digestion==== | ====Digestion==== | ||
- | ''In | + | ''by Eugene and Fabio'' |
- | ====Electrophoresis==== | + | |
- | ''In | + | In order to place the '''BBa_B0015''' just after the '''BBa_K1372000''', we will start the [http://parts.igem.org/Help:Assembly/3A_Assembly Assembly procedure] again. |
+ | * BioBrick '''BBa_K1372000''' (Salicylate promoter + NahR + RNA suppressor) as '''Part A''' | ||
+ | * BioBrick '''BBa_B0015''' (Double terminator) as '''Part B''' | ||
+ | The enzymes used were: | ||
+ | |||
+ | * '''EcoRI''' and '''SpeI''' for '''BBa_K1372000''' | ||
+ | * '''EcoRI''' and '''XbaI''' for '''BBa_B0015''' | ||
+ | |||
+ | <font color="#F00">TODO: Illustration of the process</font> | ||
+ | |||
+ | [https://2014.igem.org/Team:Paris_Saclay/Protocols/BioBrick_Assembly#Digest_reaction BioBrick Assembly - Digest Reaction Protocol] | ||
+ | ====Segregate Process by Electrophoresis==== | ||
+ | ''by Eugene and Fabio'' | ||
+ | |||
+ | # BBa_K1372000 digested by '''EcoRI''' and '''SpeI''' | ||
+ | # BBa_B0015 digested by '''EcoRI''' and '''XbaI''' | ||
+ | |||
+ | '''Results:''' | ||
+ | |||
+ | # | ||
+ | # | ||
+ | ''In progress'' | ||
+ | |||
+ | [https://2014.igem.org/Team:Paris_Saclay/Protocols/BioBrick_Assembly#Segregate_process BioBrick Assembly - Segregate Process Protocol] | ||
====Ligation==== | ====Ligation==== | ||
''In Progress'' | ''In Progress'' |
Revision as of 16:46, 6 August 2014
Contents |
Wednesday 6th August
Lab work
C - Salicylate Inducible Suppressing System
Plasmid DNA Purification
by Eugene and Fabio
- BBa_K1372000 Cl.1
- BBa_K1372000 Cl.2
From Liquid Culture made the 5th August
Digestion
by Eugene and Fabio
In order to place the BBa_B0015 just after the BBa_K1372000, we will start the [http://parts.igem.org/Help:Assembly/3A_Assembly Assembly procedure] again.
- BioBrick BBa_K1372000 (Salicylate promoter + NahR + RNA suppressor) as Part A
- BioBrick BBa_B0015 (Double terminator) as Part B
The enzymes used were:
- EcoRI and SpeI for BBa_K1372000
- EcoRI and XbaI for BBa_B0015
TODO: Illustration of the process
BioBrick Assembly - Digest Reaction Protocol
Segregate Process by Electrophoresis
by Eugene and Fabio
- BBa_K1372000 digested by EcoRI and SpeI
- BBa_B0015 digested by EcoRI and XbaI
Results:
In progress
BioBrick Assembly - Segregate Process Protocol
Ligation
In Progress
Electrophoresis
In Progress
D - Lemon scent
PCR Cleanup
by Pierre & Sean
BioBricks used: BBa_K762100 and BBa_K517003 (PCR perfomed on the 4th August)
Bibliography
By Hoang Vu
Still working on my mission: find more informations about limonene, pinene and citral A and B.
Members present:
- Instructors and advisors: Alice.
- Students: Eugene, Fabio, Hoang Vu, Juliette, Melanie, Pierre, Romain, Sean and Terry.