Team:Groningen/Labwork/23 July 2013
From 2013.igem.org
Mirjam
Run a gel with the PCR products of silk without strep + signal sequence.
The PCR of silk without strep + signal sequence is successful. A new 1.5% agarose gel is made to do gel purification. Did the gel purification.
Run a gel with the purified PCR product of silk strepF-R and silk F-strepR.
The products are present in 2/3 samples for each silk type. These are combined and concentrated. Concentrations of 18.1 and 16.1 ng/ul are obtained. So a restriction digestion can be made.
Made a restriction digestion for the signal sequences.
Sander
Made a restriction digestion for silk strepF-R and silk F-strepR.
Inne
E. coli with the BBa_818000 backbone that had to grow overnight grew.
Sample | Composition | BBa_k818000 from | growth |
1 | 4 mL LB, 8 uL Amp | iGEM 2012 | Yes |
2 | 4 mL LB, 8 uL Amp | iGEM 2012 | Yes |
3 | 4 mL, LB 8 uL Amp (negative control) | iGEM 2012 | No |
4 | 4 mL LB, 8 uL Amp, 4 uL IPTG | iGEM 2012 | Yes |
5 | 4 mL LB, 8 uL Amp, 4 uL IPTG | iGEM 2012 | Yes |
6 | 4 mL, 8uL Amp | iGEM 2013 | Yes |
7 | 4 mL, 8 uL Amp, 8uL IPTG | iGEM 2013 | Yes |
8 | 4 mL, 8 uL Amp (negative control) | iGEM 2013 | No |