"
Team:Paris Saclay/Notebook/July/29
From 2014.igem.org
(→PCR) |
(→Lab Work) |
||
| Line 93: | Line 93: | ||
|} | |} | ||
| - | + | The different bacterial cultures in each tubes: | |
| - | + | ||
| - | + | ||
| - | + | ||
| - | + | ||
| - | + | ||
| - | + | ||
| - | + | ||
| - | + | ||
#Tube 1: MG1655Z1 10I | #Tube 1: MG1655Z1 10I | ||
Revision as of 08:09, 31 July 2014
Contents |
Tuesday 29th July
Lab Work
A - The frame coli Odor free
PCR
by Romain
Strains used: E. coli MG1655Z1 and E. coli MG1655, and oligonucleotides used: FTR-Apra-F and FTR-Apra-R.
Protocol
Add into a PCR tube the following:
| Component | For a total volume of 50μl |
|---|---|
| H2O | 27.25μl |
| Green GoTaq buffer 5X | 10μl |
| dNTPs | 1μl |
| FTR-Apra-F | 2μl |
| FTR-Apra-R | 2μl |
| DMSO | 1.5μl |
| MgCl2 | 4μl |
| Bacterial culture | 2μl |
| Green GoTaq enzyme | 0.25μl |
Tube was placed in PCR machine with the following parameters.
| Cycle step | Temperature | Time | Cycle |
|---|---|---|---|
|
Initial denaturation |
95°C |
5 min |
1 |
| Denaturation | 95°C | 30 s | 30 |
| Annealing | 60°C | 30 s | 30 |
| Extension | 72°C | 2 min | 30 |
| Final extension | 72°C | 5 min | 1 |
| Final extension | 12°C | hold | 1 |
The different bacterial cultures in each tubes:
- Tube 1: MG1655Z1 10I
- Tube 2: MG1655 100II
- Tube 3: MG1655 50I
- Tube 4: MG1655 100I
- Tube 5: MG1655Z1 10II
- Tube 6: MG1655 50II
- Tube 7: MG1655Z1 10I positive control with plasmid
Results of the PCR: The electrophoresis revealed nothing
New PCR with different enyme.
Strains used: MG1655 and MG1655Z1, and oligonucleotides used: FTR-Apra-F and FTR-Apra-R.
Protocol
Add into a PCR tube the following:
| Component | For a total volume of 50μl |
|---|---|
| H2O | 37.25μl |
| DreamTaq buffer 10X | 5μl |
| dNTPs | 1μl |
| FTR-Apra-F | 1μl |
| FTR-Apra-R | 1μl |
| DMSO | 2.5μl |
| Bacterial culture | 2μl |
| DreamTaq enzyme | 0.25μl |
Tube was placed in PCR machine with the following parameters.
| Cycle step | Temperature | Time | Cycle |
|---|---|---|---|
|
Initial denaturation |
95°C |
5 min |
1 |
| Denaturation | 95°C | 30 s | 30 |
| Annealing | 60°C | 30 s | 30 |
| Extension | 72°C | 2 min | 30 |
| Final extension | 72°C | 5 min | 1 |
| Final extension | 12°C | hold | 1 |
- Tube 1: MG1655Z1 10I
- Tube 2: MG1655 100II
- Tube 3: MG1655 50I
- Tube 4: MG1655 100I
- Tube 5: MG1655Z1 10II
- Tube 6: MG1655 50II
- Tube 7: MG1655Z1 10I positive control with plasmid
Results of the PCR: The electrophoresis revealed successfully the DNA!
D - Lemon scent
PCR of BBa_K762100
by Sean
Oligonucleotides used: iPS66, iPS67
Oligonucleotides were diluted twice from 100µM to 50µM.
Protocol
Add into a PCR tube the following:
| Component | For a total volume of 50μl |
|---|---|
| H2O | 35.5μl |
| Phusion buffer 5X | 10μl |
| dNTPs | 1μl |
| iPS66 | 1μl |
| iPS67 | 1μl |
| BBa_K762100 | 1μl |
| Phusion DNA polymerase | 0.25μl |
Tube was placed in PCR machine with the following parameters.
| Cycle step | Temperature | Time | Cycle |
|---|---|---|---|
|
Initial denaturation |
98°C |
1 min |
1 |
| Denaturation | 98°C | 15 s | 25 - 30 |
| Annealing | 55°C | variable | 25 - 30 |
| Extension | 72°C | 45 s | 25-30 |
| Final extension | 72°C | 10 min | 1 |
| Final extension | 8°C | hold | 1 |
E - Salicylate Inducible Suppressing System
Digestion
by Fabio
BioBrick BBa_J61051 (Salicylate promoter + NahR)
Electrophoresis
by Fabio
Results:
First process to verify the digestion
Second one to separate both parts (only with J61051).
Members there:
- Instructors and advisors: Alice, Solenne and Sylvie.
- Students: Arnaud, Fabio, Romain, Sean and Terry.
