"
Team:Paris Saclay/Notebook/June/26
From 2013.igem.org
(Difference between revisions)
(→Lab work) |
|||
| Line 21: | Line 21: | ||
| + | {| border="1" align="center" | ||
| + | |[[Team:Paris Saclay/Notebook/June/25|<big>Previous day</big>]] | ||
| + | |||
| + | |[[Team:Paris_Saclay/Notebook|<big>Back to calendar</big>]] | ||
| + | |||
| + | |[[Team:Paris Saclay/Notebook/June/27|<big>Next day</big>]] | ||
| + | |} | ||
{{Team:Paris_Saclay/incl_fin}} | {{Team:Paris_Saclay/incl_fin}} | ||
Revision as of 09:36, 1 October 2013
Notebook : June 26
Lab work
- Design of the oligonucleotide for the amplification of Pbphr1 (intergenic sequence upstream) for Pseudomonas pseudoalcaligenes PbphD and KF707 (intergenic sequence upstream) for Burkholderia xenovorans LB400
- 500 ml Buffers (TB: the Transformation Buffer) prepared to make super competent bacteria, stored at 4°C
- 250 ml of culture of E.Coli DH5αZ1 in LB prepared for overnight culture, with an initial Do (Optical Density) of 0.04 at 17h30min
- Protocol of extraction of the genomic DNA from bacteria (E.Coli DH5α) written
- Documentation about the fnr activator operator sequences in iGEM registry
Human practices
- Team meeting and discussion with Munich team (Skype)
| Previous day | Back to calendar | Next day |
