Team:Paris Saclay/Notebook/July/8
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+ | {{Team:Paris_Saclay/notebook_header}} | ||
=Tuesday 8th July= | =Tuesday 8th July= | ||
- | |||
==Lab work== | ==Lab work== | ||
- | + | ====Rehydration of the following biobricks:==== | |
- | ==== | + | ''by Sean'' |
- | '' | + | |
* BBa_B0015(CmR) | * BBa_B0015(CmR) | ||
Line 15: | Line 14: | ||
* BBa_J23114(AmpR) | * BBa_J23114(AmpR) | ||
- | + | Protocol: | |
- | Protocol: | + | |
- | + | ||
# Pierce foil cover of well containing biobrick of interest. | # Pierce foil cover of well containing biobrick of interest. | ||
# Add 10 μl of water in well. | # Add 10 μl of water in well. | ||
# Transfer contents of well into a 1.5 ml microcentrifuge tube. | # Transfer contents of well into a 1.5 ml microcentrifuge tube. | ||
- | ==== | + | ====Transformation in DH5α of the following biobricks:==== |
- | '' | + | ''by Mathieu & Maher'' |
* BBa_B0015(CmR) | * BBa_B0015(CmR) | ||
* BBa_J23119(CmR) | * BBa_J23119(CmR) | ||
Line 34: | Line 31: | ||
* Control + : pUC18 (20ng) | * Control + : pUC18 (20ng) | ||
* Control - | * Control - | ||
- | |||
[https://2014.igem.org/Team:Paris_Saclay/Protocols/Transformation_of_supercompetent_Ecoli_cells Protocol] | [https://2014.igem.org/Team:Paris_Saclay/Protocols/Transformation_of_supercompetent_Ecoli_cells Protocol] | ||
- | 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. | + | NB : The protocol was modified. Instead of spreading 10<sup>-1</sup> and 10<sup>-2</sup> solutions of bacteria we took a non diluted solution and a 10<sup>-1</sup> solution. |
- | ==== | + | ====Plasmid DNA preparation:==== |
- | + | ''by Romain & Sean'' | |
- | '' | + | |
Plasmids used: | Plasmids used: | ||
* pJBEI-6409 | * pJBEI-6409 | ||
- | |||
''E. coli'' strain used: | ''E. coli'' strain used: | ||
Line 53: | Line 47: | ||
[https://2014.igem.org/Team:Paris_Saclay/Protocols/Extraction_of_the_Genomic_DNA_from_Bacteria_by_using_NucleoSpin%C2%AE_Tissue Protocol] | [https://2014.igem.org/Team:Paris_Saclay/Protocols/Extraction_of_the_Genomic_DNA_from_Bacteria_by_using_NucleoSpin%C2%AE_Tissue Protocol] | ||
- | [ | + | |
+ | ==Photo of the Day== | ||
+ | [[File:Paris Saclay 8_july.jpg|600px|center]] | ||
+ | |||
+ | '''Members present:''' | ||
+ | * Instructors and advisors: Alice, Solenne and Sylvie. | ||
+ | * Students: Arnaud, Fabio, Juliette, Maher, Marie, Mathias, Mathieu, Pierre, Romain and Sean. | ||
+ | |||
+ | {{Team:Paris_Saclay/notebook_footer}} |
Latest revision as of 15:36, 14 October 2014
Contents |
Tuesday 8th July
Lab work
Rehydration of the following biobricks:
by 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.
Transformation in DH5α of the following biobricks:
by 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.
Plasmid DNA preparation:
by Romain & Sean
Plasmids used:
- pJBEI-6409
E. coli strain used:
- XL1-Blue
Photo of the Day
Members present:
- Instructors and advisors: Alice, Solenne and Sylvie.
- Students: Arnaud, Fabio, Juliette, Maher, Marie, Mathias, Mathieu, Pierre, Romain and Sean.