Team:Paris Saclay/Notebook/July/8
From 2014.igem.org
(Difference between revisions)
(→2 - Transformation in DH5α of the following biobricks:) |
(→Tuesday 8th July) |
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Line 6: | Line 6: | ||
'''Sean''' | '''Sean''' | ||
- | * | + | * BBa_B0015(CmR) |
- | * | + | * BBa_J23119(CmR) |
- | * | + | * BBa_K731020(CmR) |
- | * | + | * BBa_K206000(CmR) |
- | * | + | * BBa_J04500(CmR) |
- | * | + | * BBa_J23100(AmpR) |
- | * | + | * BBa_J23106(AmpR) |
- | * | + | * BBa_J23114(AmpR) |
Line 19: | Line 19: | ||
# Pierce foil cover of well containing biobrick of interest. | # Pierce foil cover of well containing biobrick of interest. | ||
- | # Add 10 | + | # Add 10 μl of water in well. |
- | # Transfer contents of well into a 1.5 | + | # Transfer contents of well into a 1.5 ml microcentrifuge tube. |
====2 - Transformation in DH5α of the following biobricks:==== | ====2 - Transformation in DH5α of the following biobricks:==== | ||
'''Mathieu & Maher''' | '''Mathieu & Maher''' | ||
- | * | + | * BBa_B0015(CmR) |
- | * | + | * BBa_J23119(CmR) |
- | * | + | * BBa_K731020(CmR) |
- | * | + | * BBa_K206000(CmR) |
- | * | + | * BBa_J04500(CmR) |
- | * | + | * BBa_J23100(AmpR) |
- | * | + | * BBa_J23106(AmpR) |
- | * | + | * BBa_J23114(AmpR) |
* Control + : pUC18 (20ng) | * Control + : pUC18 (20ng) | ||
* Control - | * Control - |
Revision as of 13:02, 24 July 2014
Contents |
Tuesday 8th July
Lab work
1 - Rehydration of the following biobricks:
Sean
- BBa_B0015(CmR)
- BBa_J23119(CmR)
- BBa_K731020(CmR)
- BBa_K206000(CmR)
- BBa_J04500(CmR)
- BBa_J23100(AmpR)
- BBa_J23106(AmpR)
- BBa_J23114(AmpR)
Protocol:
- Pierce foil cover of well containing biobrick of interest.
- Add 10 μl of water in well.
- Transfer contents of well into a 1.5 ml microcentrifuge tube.
2 - Transformation in DH5α of the following biobricks:
Mathieu & Maher
- BBa_B0015(CmR)
- BBa_J23119(CmR)
- BBa_K731020(CmR)
- BBa_K206000(CmR)
- BBa_J04500(CmR)
- BBa_J23100(AmpR)
- BBa_J23106(AmpR)
- BBa_J23114(AmpR)
- Control + : pUC18 (20ng)
- Control -
NB : The protocol was modified. Instead of spreading 10-1 and 10-2 solutions of bacteria we took a non diluted solution and a 10-1 solution.
3 - Plasmid DNA preparation:
Romain & Sean
Plasmids used:
- pJBEI-6409
E. coli strain used:
- XL1-Blue