Team:Paris Saclay/Notebook/August/22
From 2014.igem.org
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=Friday 22nd August= | =Friday 22nd August= | ||
==Lab work== | ==Lab work== | ||
- | === | + | ===Lemon Scent=== |
====pPSI digestion==== | ====pPSI digestion==== | ||
Line 25: | Line 25: | ||
====pPSI dephosphorylation==== | ====pPSI dephosphorylation==== | ||
+ | |||
+ | [[File:Paris_Saclay_140822.jpg|left]] | ||
After 2 hours, add 1.5µL of Alkaline Phosphatase (AP) and let it 1 hour. | After 2 hours, add 1.5µL of Alkaline Phosphatase (AP) and let it 1 hour. | ||
Line 32: | Line 34: | ||
We've made a electrophoresis to check the digestion. | We've made a electrophoresis to check the digestion. | ||
- | + | '''Legend''' | |
+ | #pPSI+Apra digested via PacI, dephosphorylated 5µl | ||
+ | #pPSI+Apra digested via PacI, dephosphorylated 5µl | ||
+ | #ladder 5µl | ||
- | ==== Ligation of BBa_K517003, BBa_K762100, and | + | ==== Ligation of BBa_K517003, BBa_K762100, and Geraniol synthase in pPSI==== |
{| class="wikitable centre" width="25%" | {| class="wikitable centre" width="25%" | ||
Line 81: | Line 86: | ||
{| class="wikitable centre" width="25%" | {| class="wikitable centre" width="25%" | ||
- | |+ | + | |+ Geraniol Synthase (GS) |
|- | |- | ||
! scope=col | components | ! scope=col | components | ||
! scope=col | volumes | ! scope=col | volumes | ||
|- | |- | ||
- | | | + | |GS |
|10μl | |10μl | ||
|- | |- | ||
Line 119: | Line 124: | ||
Finally put it in a incubator at 37°C for 30 minutes | Finally put it in a incubator at 37°C for 30 minutes | ||
+ | |||
+ | |||
+ | |||
+ | ====PCR of CAD ==== | ||
+ | With or synthetic gene, we decided to do a PCR to have more matrice. | ||
+ | |||
+ | {| class="wikitable centre" width="25%" | ||
+ | |+ In one tube | ||
+ | |- | ||
+ | ! scope=col | components | ||
+ | ! scope=col | volumes | ||
+ | |- | ||
+ | |H<sub>2</sub>O | ||
+ | |27μl | ||
+ | |- | ||
+ | |5x phusion buffer | ||
+ | |2µl | ||
+ | |- | ||
+ | |dNTP 10 mM | ||
+ | |2µl | ||
+ | |- | ||
+ | |iPS83 10µM | ||
+ | |5µl | ||
+ | |- | ||
+ | |iPS84 10µM | ||
+ | |5µl | ||
+ | |- | ||
+ | |DMSO | ||
+ | |1.5µl | ||
+ | |} | ||
+ | |||
+ | ====PCR purification==== | ||
+ | We use the kit PCR clean-up | ||
+ | |||
+ | the elution volume is 20µl | ||
+ | |||
+ | {| class="wikitable centre" width="25%" | ||
+ | |+ kit PCR clean-up | ||
+ | ! scope=col | DNA Polymerase | ||
+ | ! scope=col | volume | ||
+ | |- | ||
+ | |Phusion | ||
+ | |0.5µl | ||
+ | |- | ||
+ | |} | ||
+ | |||
+ | {| class="wikitable centre" width="25%" | ||
+ | |+ PCR cycle | ||
+ | |- | ||
+ | ! scope=col | Temperature (°C) | ||
+ | ! scope=col | time | ||
+ | |- | ||
+ | |98 | ||
+ | |30 sec | ||
+ | |- | ||
+ | |98 | ||
+ | |10 sec | ||
+ | |- | ||
+ | |58 | ||
+ | |30 sec | ||
+ | |- | ||
+ | |72 | ||
+ | |45 sec | ||
+ | |- | ||
+ | |72 | ||
+ | |10 min | ||
+ | |- | ||
+ | |} | ||
+ | |||
+ | ==Photo of the Day== | ||
+ | [[File:Paris Saclay 22_august.jpg|600px|center]] | ||
+ | |||
+ | '''Members present:''' | ||
+ | * Instructors and advisors: Alice, Solenne and Sylvie. | ||
+ | * Students: Eugène, Hoang Vu, Laëtitia, Mélanie, Romain, Sean and Terry. | ||
{{Team:Paris_Saclay/notebook_footer}} | {{Team:Paris_Saclay/notebook_footer}} |
Latest revision as of 15:10, 14 October 2014
Contents |
Friday 22nd August
Lab work
Lemon Scent
pPSI digestion
components | volumes |
---|---|
pPSI | 40μl |
FastDigest green buffer 10X | 5μl |
PacI | 2µl |
H2O | 2µl |
pPSI dephosphorylation
After 2 hours, add 1.5µL of Alkaline Phosphatase (AP) and let it 1 hour.
Then, inactivation of AP at 65°C during 15 minutes.
We've made a electrophoresis to check the digestion.
Legend
- pPSI+Apra digested via PacI, dephosphorylated 5µl
- pPSI+Apra digested via PacI, dephosphorylated 5µl
- ladder 5µl
Ligation of BBa_K517003, BBa_K762100, and Geraniol synthase in pPSI
components | volumes |
---|---|
BBa_K517003 | 10μl |
pPSI | 2μl |
buffer | 2µl |
H2O | 5µl |
ligase | 1µl |
components | volumes |
---|---|
BBa_K762100 | 10μl |
pPSI | 2μl |
buffer | 2µl |
H2O | 5µl |
ligase | 1µl |
components | volumes |
---|---|
GS | 10μl |
pPSI | 2μl |
buffer | 2µl |
H2O | 5µl |
ligase | 1µl |
And let it in the freezer for 3 hours.
Transformation in competent E.coli DH5α
After 3 hours, take out the ligation tubes and add 100 µl of competent DH5α in each tube.
Then proceed to the transformation protocol.
- 20 minutes at 4°C
- 2 minutes 30 seconds at 42°C
- 2 minutes at 4 °C
- Add 0.9 ml of LB into the tubes
Finally put it in a incubator at 37°C for 30 minutes
PCR of CAD
With or synthetic gene, we decided to do a PCR to have more matrice.
components | volumes |
---|---|
H2O | 27μl |
5x phusion buffer | 2µl |
dNTP 10 mM | 2µl |
iPS83 10µM | 5µl |
iPS84 10µM | 5µl |
DMSO | 1.5µl |
PCR purification
We use the kit PCR clean-up
the elution volume is 20µl
DNA Polymerase | volume |
---|---|
Phusion | 0.5µl |
Temperature (°C) | time |
---|---|
98 | 30 sec |
98 | 10 sec |
58 | 30 sec |
72 | 45 sec |
72 | 10 min |
Photo of the Day
Members present:
- Instructors and advisors: Alice, Solenne and Sylvie.
- Students: Eugène, Hoang Vu, Laëtitia, Mélanie, Romain, Sean and Terry.