Team:DTU-Denmark/Notebook/6 August 2013
From 2013.igem.org
(→Gel purification) |
|||
(9 intermediate revisions not shown) | |||
Line 1: | Line 1: | ||
{{:Team:DTU-Denmark/Templates/StartPage|6 August 2013}} | {{:Team:DTU-Denmark/Templates/StartPage|6 August 2013}} | ||
- | |||
Navigate to the [[Team:DTU-Denmark/Notebook/5_August_2013|Previous]] or the [[Team:DTU-Denmark/Notebook/7_August_2013|Next]] Entry | Navigate to the [[Team:DTU-Denmark/Notebook/5_August_2013|Previous]] or the [[Team:DTU-Denmark/Notebook/7_August_2013|Next]] Entry | ||
=Lab 208= | =Lab 208= | ||
Line 6: | Line 5: | ||
==Main purpose== | ==Main purpose== | ||
<hr/> | <hr/> | ||
- | * PCR for AMO | + | * Extraction PCR for AMO |
* PCR for SPL (synthetic promoter library) | * PCR for SPL (synthetic promoter library) | ||
* PCR for reference promoter | * PCR for reference promoter | ||
* PCR for araBAD biobrick K808000 | * PCR for araBAD biobrick K808000 | ||
- | * PCR to extract Nir2 from P. aeruginosa | + | * PCR to extract Nir2 from ''P. aeruginosa'' |
* PCR for araBAD and SPL with DMSO | * PCR for araBAD and SPL with DMSO | ||
* PCR on Nir1 with MgCl2 gradient | * PCR on Nir1 with MgCl2 gradient | ||
- | * Gel purification | + | * Gel purification of Nir1 (from ''P. aeruginosa'') |
- | * Plasmid | + | * Plasmid isolation: HAO in pZA21 from USER cloning. |
==Who was in the lab== | ==Who was in the lab== | ||
Line 31: | Line 30: | ||
===PCR for SPL (synthetic promoter library)=== | ===PCR for SPL (synthetic promoter library)=== | ||
- | template: | + | template: pZA21 with RFP, primers: 52a, 52b1, temperature: 50C, time: 2:30 |
===PCR for reference promoter=== | ===PCR for reference promoter=== | ||
- | template: | + | template: pZA21 with RFP, primers: 52a, 52b2, temperature: 50C, time: 2:30 |
===PCR for araBAD K808000=== | ===PCR for araBAD K808000=== | ||
Line 134: | Line 133: | ||
==Conclusion== | ==Conclusion== | ||
<hr/> | <hr/> | ||
+ | *Nir was obtained from colony PCR and purified. | ||
+ | *AMO was extracted and gel purified. | ||
Navigate to the [[Team:DTU-Denmark/Notebook/5_August_2013|Previous]] or the [[Team:DTU-Denmark/Notebook/7_August_2013|Next]] Entry | Navigate to the [[Team:DTU-Denmark/Notebook/5_August_2013|Previous]] or the [[Team:DTU-Denmark/Notebook/7_August_2013|Next]] Entry | ||
{{:Team:DTU-Denmark/Templates/EndPage}} | {{:Team:DTU-Denmark/Templates/EndPage}} |
Latest revision as of 22:09, 29 September 2013
6 August 2013
Contents |
Lab 208
Main purpose
- Extraction PCR for AMO
- PCR for SPL (synthetic promoter library)
- PCR for reference promoter
- PCR for araBAD biobrick K808000
- PCR to extract Nir2 from P. aeruginosa
- PCR for araBAD and SPL with DMSO
- PCR on Nir1 with MgCl2 gradient
- Gel purification of Nir1 (from P. aeruginosa)
- Plasmid isolation: HAO in pZA21 from USER cloning.
Who was in the lab
Kristian, Gosia, Natalia, Henrike
Procedure
PCR for AMO
Made four reactions using 1 uL respectively 10 uL of culture from the -20 or from the glycerol stock (-80) as template and adjusted volume of water accordingly.
Primers 10a, 10b.
PCR for SPL (synthetic promoter library)
template: pZA21 with RFP, primers: 52a, 52b1, temperature: 50C, time: 2:30
PCR for reference promoter
template: pZA21 with RFP, primers: 52a, 52b2, temperature: 50C, time: 2:30
PCR for araBAD K808000
template: K808000, primers: 12a, 12bn, temperature: 50C, time: 2:30
PCR to extract Nir2 from P. aeruginosa
PCR for araBAD and SPL with DMSO
Template and primers as previous.
PCR on Nir1 with MgCl2 gradient
Used previous isolation from a gel purification to make PCR for amplification of the strand. Used 5% DMSO as additive. The PCR was done with primer pair 41 and with x7 polymerase at 55C annealing and 5:00 min extension. Also we used 20 sec as denaturing time instead of the normal 10. The magnesium gradient was as follow:
- 0
- 1uL MgCl2 2mM per 50uL reaction
- 5uL MgCl2 2mM per 50uL reaction
- 20uL MgCl2 2mM per 50uL reaction
Gel purification
of the Nir1 fragment extracted from P. aeruginosa. Nanodrop: 8ng/uL
Plasmid miniprep
HAO in pZA21 from USER cloning was purified for restriction analysis. Nanodrop measurement: 180ng/uL
Results
Gel 1
1% agarose gel
- 1 kb ladder
- Nir1 col. Taq
- Nir1 col. Taq
- Nir2 col. Taq
- Nir2 col. Taq
- Nir1 frag. Taq
- Nir1 frag. Taq
- Nir1 col. x7
- Nir1 col. x7
- neg
- Hi spec. buffer
- Hi spec. buffer
- DMSO
- DMSO
- Nir1
- Nir1
- Nir2
- Nir2
- 1 kb ladder
Nir1 was purified.
Gel 2
1% agarose gel
- 1 kb ladder
- NirW
- NirW
- araBAD biobrick K808000
- araBAD biobrick K808000
- SPL in pZA21 containing RFP
- SPL in pZA21 containing RFP
- reference promoter in pZA21 containing RFP
- reference promoter in pZA21 containing RFP
- neg
- neg
- 1 kb ladder
Gel 3
1% agarose gel
- 1 kb ladder
- AMO, 1uL of -20 culture as template
- AMO, 10uL of -20 culture as template
- AMO, 1uL of glycerol stock as template
- AMO, 10uL of glycerol stock as template
- neg from AMO PCR
- 1 - SPL, primers 52a, 52b1, template pZA21 with RFP, 50C, 2:30 min extension
- 2 - SPL, primers 52a, 52b1, template pZA21 with RFP, 50C, 2:30 min extension
- 3 - ref, primers 52a, 52b2, template pZA21 with RFP, 50C, 2:30 min extension
- 4 - ref, primers 52a, 52b2, template pZA21 with RFP, 50C, 2:30 min extension
- 5 - araBAD, primers 12a, 12bn, template K80800, 50C, 2:30 min extension
- 6 - araBAD, primers 12a, 12bn, template K80800, 50C, 2:30 min extension
- 1 kb ladder
AMO was gel purified.
Conclusion
- Nir was obtained from colony PCR and purified.
- AMO was extracted and gel purified.
Navigate to the Previous or the Next Entry