Team:Groningen/Labwork/18 July 2013
From 2013.igem.org
(Difference between revisions)
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<br>Both negative controls were clear, and the rest of the samples was turbid. | <br>Both negative controls were clear, and the rest of the samples was turbid. | ||
<br>Did a miniprep of the samples 1 & 2 (the ones with Amp). | <br>Did a miniprep of the samples 1 & 2 (the ones with Amp). | ||
+ | <table border="1"> | ||
+ | <tr> | ||
+ | <td>#</td> | ||
+ | <td>composition</td> | ||
+ | <td>Bacteria</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>1</td> | ||
+ | <td>4mL LB 8uL Amp</td> | ||
+ | <td>+</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>2</td> | ||
+ | <td>4mL LB 8uL Amp</td> | ||
+ | <td>+</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>3</td> | ||
+ | <td>4mL LB 8uL Amp (negative control)</td> | ||
+ | <td>-</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>4</td> | ||
+ | <td>4mL LB</td> | ||
+ | <td>+</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>5</td> | ||
+ | <td>4mL LB (negative control)</td> | ||
+ | <td>-</td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | |||
<br>Afterwards concentration of DNA was determined via nanodrop. | <br>Afterwards concentration of DNA was determined via nanodrop. | ||
Revision as of 11:17, 18 July 2013
Sander
prepared 20 tubes for use in -80 c Glyserol stock
Inne & Mirjam
Cells with BBa_k818000, inoculated overnight, were successfully grown.
Both negative controls were clear, and the rest of the samples was turbid.
Did a miniprep of the samples 1 & 2 (the ones with Amp).
# | composition | Bacteria |
1 | 4mL LB 8uL Amp | + |
2 | 4mL LB 8uL Amp | + |
3 | 4mL LB 8uL Amp (negative control) | - |
4 | 4mL LB | + |
5 | 4mL LB (negative control) | - |
Afterwards concentration of DNA was determined via nanodrop.
Results: sample 1 = 60.1 ng/uL, sample 2 = 31.8 ng/uL
During the miniprep the filtered LB medium was poured back into the culture (so cells could grow again).
A -80 C stock was made with 1 mL culture (sample 1). (stored in tray: iGEM 2012 A, compartment 70)