Team:Groningen/Notebook/Wetwork 25August2012

From 2012.igem.org

(Difference between revisions)
Line 10: Line 10:
The different restricted DNA fragments were analysed on an agarose gel and removed from it. The obtained gel fragment was purified. For the ligation an end volume of 10 ul was used. 8.5 ul was used for the backbone and the template. Approximately ratio of backbone and template was 2:3:3. Ligation was incubated at 22 degrees celcius for two hours. Obtained DNA was transformed into E. coli.
The different restricted DNA fragments were analysed on an agarose gel and removed from it. The obtained gel fragment was purified. For the ligation an end volume of 10 ul was used. 8.5 ul was used for the backbone and the template. Approximately ratio of backbone and template was 2:3:3. Ligation was incubated at 22 degrees celcius for two hours. Obtained DNA was transformed into E. coli.
 +
Tom/Renske
 +
 +
PCR amplification of promoters+GFPopt:
 +
 +
1) AlsT 300_GFP: FW Alst300 + RV GFP
 +
 +
2) Alst 500_GFP: FW Alst500 RV GFP
 +
 +
3) combine FNR+GFP: FW FNR, RV GFP
 +
 +
4) AlsT250: FWAlst250_RV GFP
 +
 +
5) AlsT150: FW Alst150, RV GFP
<html>
<html>
<A HREF="https://2012.igem.org/Team:Groningen/Notebook"><FONT COLOR=#ff6700>Back to notebook</FONT></A>
<A HREF="https://2012.igem.org/Team:Groningen/Notebook"><FONT COLOR=#ff6700>Back to notebook</FONT></A>

Revision as of 12:58, 21 September 2012





Emeraldo/Tom

Ligation of alsT 300, Fnr and s-box promotor to GFP and lycopene in Psac with a new protocol. Psac was digested with EcorI. Fnr, alsT 300 and s-box were digested with EcorI and SpeI. Lycopene and GFP were digested with PstI and XbaI. Reaction was incubated for 2 hours at 37 degrees celcius.

The different restricted DNA fragments were analysed on an agarose gel and removed from it. The obtained gel fragment was purified. For the ligation an end volume of 10 ul was used. 8.5 ul was used for the backbone and the template. Approximately ratio of backbone and template was 2:3:3. Ligation was incubated at 22 degrees celcius for two hours. Obtained DNA was transformed into E. coli.

Tom/Renske

PCR amplification of promoters+GFPopt:

1) AlsT 300_GFP: FW Alst300 + RV GFP

2) Alst 500_GFP: FW Alst500 RV GFP

3) combine FNR+GFP: FW FNR, RV GFP

4) AlsT250: FWAlst250_RV GFP

5) AlsT150: FW Alst150, RV GFP Back to notebook

Our sponsors: