Team:Paris Saclay/Notebook/August/20
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(Difference between revisions)
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Used quantities : | Used quantities : | ||
- | * | + | * Oligo 54F : 2µL |
+ | * Oligo 55R : 2µL | ||
+ | * DNA : 1µL | ||
+ | * Buffer Phusion : 10µL | ||
+ | * dNTP : 1µL | ||
+ | * Phusion : 1µL | ||
+ | * DMS9 : 2µL ?????????????????????????????????? | ||
+ | * H2O : 31µL | ||
- | PCR | + | PCR program : |
+ | |||
+ | [[File:Pstest.jpg|400px]] | ||
===='''2 - Electrophoresis of PCR products : BphR2 Part I'''==== | ===='''2 - Electrophoresis of PCR products : BphR2 Part I'''==== | ||
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{| | {| | ||
| style="border:1px solid black;padding:5px;background-color:#DEDEDE;" | | | style="border:1px solid black;padding:5px;background-color:#DEDEDE;" | | ||
- | + | We lost our fragment. We will do the PCR again. | |
|} | |} | ||
{{Team:Paris_Saclay/incl_fin}} | {{Team:Paris_Saclay/incl_fin}} |
Revision as of 19:04, 20 September 2013
Contents |
Notebook : August 20
Lab work
A - Aerobic/Anaerobic regulation system
Objective : obtaining Bba_K1155004, Bba_K1155005, Bba_K1155006
1 - Sequences analysis
Damir, XiaoJing
...
A - Aerobic/Anaerobic regulation system / B - PCB sensor system
Objective : obtaining FNR and BphR2 proteins
1 - PCR of BphR2 Part I
Damir
Used quantities :
- Oligo 54F : 2µL
- Oligo 55R : 2µL
- DNA : 1µL
- Buffer Phusion : 10µL
- dNTP : 1µL
- Phusion : 1µL
- DMS9 : 2µL ??????????????????????????????????
- H2O : 31µL
PCR program :
2 - Electrophoresis of PCR products : BphR2 Part I
Nadia
[[]] |
|
We obtain a frangment at the right size. We can purify it. |
2 - Gel purification of PCR products : BphR2 Part I
Damir, Nadia
Protocol : Gel purification
Nanodrop :
- BphR2 Part I: .........
We lost our fragment. We will do the PCR again. |