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Team:Paris Bettencourt/Notebook/Phage Sensor/Monday 15th July.html
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| - | We made a 1:1000 | + | We made a 1:1000 dilution of KAN (stand.c) in an LB solid media.<br> |
| - | + | <br> | |
| + | Pouring the plates. Around 20 mL/plate<br> | ||
1. KEIOΔPYR KANR Growth<br> | 1. KEIOΔPYR KANR Growth<br> | ||
2. ME1655 KANR No growth<br> | 2. ME1655 KANR No growth<br> | ||
| Line 19: | Line 20: | ||
<br> | <br> | ||
The KEIOΔPYRF growed as expected. Negative control did not growth.<br> | The KEIOΔPYRF growed as expected. Negative control did not growth.<br> | ||
| - | |||
Plates have KAN antibiotic<br> | Plates have KAN antibiotic<br> | ||
KEIO has KAN R.<br> | KEIO has KAN R.<br> | ||
Latest revision as of 16:39, 22 August 2013
Phage Sensor
ASDFMonday 15th July
Plating and control of antibiotic resistance.
We made a 1:1000 dilution of KAN (stand.c) in an LB solid media.Pouring the plates. Around 20 mL/plate
1. KEIOΔPYR KANR Growth
2. ME1655 KANR No growth
Conclusion :
The KEIOΔPYRF growed as expected. Negative control did not growth.
Plates have KAN antibiotic
KEIO has KAN R.
