Team:Paris Saclay/Notebook/August/12
From 2013.igem.org
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{{Team:Paris_Saclay/incl_debut_generique}} | {{Team:Paris_Saclay/incl_debut_generique}} | ||
- | ='''Notebook : August | + | ='''Notebook : August 12'''= |
=='''Lab work'''== | =='''Lab work'''== | ||
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==='''A - Aerobic/Anaerobic regulation system'''=== | ==='''A - Aerobic/Anaerobic regulation system'''=== | ||
- | ===='''1 - | + | Obtaining Pfnr_RBS-LacZ-Term in PSB1C3 |
+ | |||
+ | ===='''1 - Digestion of Bba_K1155000, Bba_K1155007 and Bba_K1155003'''==== | ||
Anaïs, Nadia, XiaoJing | Anaïs, Nadia, XiaoJing | ||
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Protocol : [[Team:Paris_Saclay/Protocols/digestion|digestion]] | Protocol : [[Team:Paris_Saclay/Protocols/digestion|digestion]] |
Revision as of 15:35, 12 August 2013
Contents |
Notebook : August 12
Lab work
A - Aerobic/Anaerobic regulation system
Obtaining Pfnr_RBS-LacZ-Term in PSB1C3
1 - Digestion of Bba_K1155000, Bba_K1155007 and Bba_K1155003
Anaïs, Nadia, XiaoJing
Protocol : digestion
10µl,50µl and 100µl petri dishes are clear so phages are multiplied.
We let the antibiotic over night to select the right strain.
2 - Obtaining RBS_lacZ_ter.
Abdou
Clone 10,14 and 15 plamid extraction using nucleospin kit.
Protocol : hight copy plamid extraction
Results: concentration measured by nanodrop
- clone 10: C=38ng/µl 260/280= 1.78
- clone 14: C=48.5ng/µl 260/280=1.90
- clone 15: C=52 ng/µl 260/280=1.78
We still have to sequence plasmids in order to verify our results.
A - Aerobic/Anaerobic regulation system / B - PCB sensing system
1 - Gibson assembly.
August 1st PCR purification to be sure about the experiment. BphR2 part1, BphR2 part2 and RBS_BphR2_part1, FNR part1, FNR part2 and RBS_FNR_part1.
Protocol : PCR_clean_up
Results:
IMAGE |
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we have no fragment so we must do again these PCRs