Team:Paris Saclay/Notebook/September/3
From 2014.igem.org
(Difference between revisions)
(→pPS3 and pPS4) |
(→pPS3 and pPS4) |
||
Line 98: | Line 98: | ||
[[File:0309 digestion HindIII pPS3 4.jpg|500px]] | [[File:0309 digestion HindIII pPS3 4.jpg|500px]] | ||
+ | |||
+ | well 1 = ladder | ||
+ | well 2-3-4 = pPS3 | ||
+ | Well 5-6-7 = pPS4 | ||
results are very strange | results are very strange |
Revision as of 11:48, 7 September 2014
Contents |
LabWork
B- Construction of the fusion protein
We made a classic exttraction of plasmids from the liquid cultures.
Check by electrophoresis if it worked and send it for sequencing.
D- Lemon scent
by Mélanie
PCR LS
Electrophoresis of the PCR made Yesterday
[photo]
The PCR have success so I use the PCR clean up kit to purify it
[photo] Electrophoresis after purification
Ligation
We already have some pPSI digested and dephosphorelated
So I do a ligation:
component | volume |
---|---|
H2O | 5μl |
buffer | 2μl |
ligase | 1μl |
pPSI | 2μl |
LS PCR | 10μl |
2 hours at room temperature and over night at 4°
pPS5
Plasmid exctraction using the kit digestion by SalI
component | volume |
---|---|
H2O | 11μl |
buffer | 5μl |
SalI | 2μl |
pPS5 | 30μl |
Electrophoresis
[photo]
We saw that we have something strang with our plasmid
pPS3 and pPS4
We digest the plasmid by HindIII to direct our insert
component | volume |
---|---|
H2O | 6μl |
buffer | 1μl |
HindIII | 1μl |
pPS3/4 | 2μl |
well 1 = ladder well 2-3-4 = pPS3 Well 5-6-7 = pPS4
results are very strange