Team:Groningen/Labwork/18 July 2013
From 2013.igem.org
(Difference between revisions)
Line 2: | Line 2: | ||
<br/>prepared 20 tubes for use in -80 c Glyserol stock. | <br/>prepared 20 tubes for use in -80 c Glyserol stock. | ||
<br/>created a restriction digest reaction for silk. | <br/>created a restriction digest reaction for silk. | ||
+ | <table border="1"> | ||
+ | <tr> | ||
+ | <td>Sample</td> | ||
+ | <td>componant</td> | ||
+ | <td>volume (ul) <td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>silk1</td> | ||
+ | <td>silk</td> | ||
+ | <td>4</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td></td> | ||
+ | <td>BamHI buffer</td> | ||
+ | <td>2</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td></td> | ||
+ | <td>BamHI enzyme</td> | ||
+ | <td>0,5</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td></td> | ||
+ | <td>BSA</td> | ||
+ | <td>0,5</td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | <br/>MilliQ was added to reach a 20 ul volume. | ||
+ | <br/> placesin incubater at 37,2 C at 17:10 | ||
Revision as of 15:18, 18 July 2013
Sander
prepared 20 tubes for use in -80 c Glyserol stock.
created a restriction digest reaction for silk.
Sample | componant | volume (ul) | |
silk1 | silk | 4 | |
BamHI buffer | 2 | ||
BamHI enzyme | 0,5 | ||
BSA | 0,5 |
MilliQ was added to reach a 20 ul volume.
placesin incubater at 37,2 C at 17:10
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)