Team:TU Delft/11 June 2010 content
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- | + | =Lab work= | |
- | + | ==BioBrick stocks== | |
Today we performed a [[Team:TU_Delft/protocols/mini-prep_plasmid_isolation|Qiagen Mini-prep plasmid isolation]] of the [https://2010.igem.org/Team:TU_Delft#/blog?blog=8_June_2010 vectors] we grew overnight. We saved 3 mL of the bacterial cells to make [[Team:TU_Delft/protocols/freezing_bacterial_stocks|-80 °C stocks]]. | Today we performed a [[Team:TU_Delft/protocols/mini-prep_plasmid_isolation|Qiagen Mini-prep plasmid isolation]] of the [https://2010.igem.org/Team:TU_Delft#/blog?blog=8_June_2010 vectors] we grew overnight. We saved 3 mL of the bacterial cells to make [[Team:TU_Delft/protocols/freezing_bacterial_stocks|-80 °C stocks]]. | ||
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- | + | ==Characterization of Anderson RBS sequences== | |
Next to that we also started digesting the first parts we will be characterizing. | Next to that we also started digesting the first parts we will be characterizing. | ||
- | ==Spring Workshop | + | ==Strain Characterization== |
+ | By Hugo | ||
+ | |||
+ | I prepared the cell bank according to the following procedure: | ||
+ | |||
+ | * Spin 5 ml of the overnight culture | ||
+ | * Add 500 ul of LB medium | ||
+ | * Add 500 ul of 80% glycerol | ||
+ | * Store the tube at -80ºC | ||
+ | |||
+ | Now, we have a cell bank ready to be used!!! | ||
+ | |||
+ | =Spring Workshop= | ||
Almost the whole team left for the iGEM spring workshop in Évry, Paris. The drive for some of us was a bit laborious (traffic jams at the middle of the night/closed roads etc.), and others actually watched the World Cup soccer match... But in the end we all arrived at the hotel in Évry little before 2 AM, Saturday morning, and got some well deserved sleep. | Almost the whole team left for the iGEM spring workshop in Évry, Paris. The drive for some of us was a bit laborious (traffic jams at the middle of the night/closed roads etc.), and others actually watched the World Cup soccer match... But in the end we all arrived at the hotel in Évry little before 2 AM, Saturday morning, and got some well deserved sleep. |
Latest revision as of 16:09, 25 August 2010
Contents |
Lab work
BioBrick stocks
Today we performed a Qiagen Mini-prep plasmid isolation of the vectors we grew overnight. We saved 3 mL of the bacterial cells to make -80 °C stocks.
The following plasmid concentrations were obtained:
BioBrick | Concentration (ng/μL) |
pSB3T5 | 266.0 |
pSB1T3 | 414.0 |
pSB1C3 | 284.7 |
pSB3C5 | 329.3 |
pSB1K3 | 270.1 |
pSB1A3 | 271.9 |
I13401 | 232.1 |
Characterization of Anderson RBS sequences
Next to that we also started digesting the first parts we will be characterizing.
Strain Characterization
By Hugo
I prepared the cell bank according to the following procedure:
- Spin 5 ml of the overnight culture
- Add 500 ul of LB medium
- Add 500 ul of 80% glycerol
- Store the tube at -80ºC
Now, we have a cell bank ready to be used!!!
Spring Workshop
Almost the whole team left for the iGEM spring workshop in Évry, Paris. The drive for some of us was a bit laborious (traffic jams at the middle of the night/closed roads etc.), and others actually watched the World Cup soccer match... But in the end we all arrived at the hotel in Évry little before 2 AM, Saturday morning, and got some well deserved sleep.