Team:DTU-Denmark/Notebook/12 August 2013
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==Procedure== | ==Procedure== | ||
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- | === Screening PCR on pZA21: | + | === Screening PCR on pZA21:araBAD:RFP spl=== |
8 different conditions and 12 different annealing temperatures were screened. | 8 different conditions and 12 different annealing temperatures were screened. | ||
* PCR mix according to [[Team:DTU-Denmark/Methods/PCR-mix| standard protocol]] with different amounts of water according to the amounts of DMSO and MgCl2 added to the reactions. | * PCR mix according to [[Team:DTU-Denmark/Methods/PCR-mix| standard protocol]] with different amounts of water according to the amounts of DMSO and MgCl2 added to the reactions. | ||
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# 5% DMSO + 1uL MgCl2 50mM + HF buffer | # 5% DMSO + 1uL MgCl2 50mM + HF buffer | ||
# 5% DMSO + 1uL MgCl2 2mM + HF buffer | # 5% DMSO + 1uL MgCl2 2mM + HF buffer | ||
- | + | * Primers - 51a and 51b1 | |
+ | * Template - "Ara" sample (plasmid isolation pZA21:araBAD:RFP). | ||
+ | * Annealing temperature: each condition were run in 12 different annealing temperatures with constant interval within the range 51 C-65 C. | ||
+ | |||
=== PCR mix for backbone=== | === PCR mix for backbone=== | ||
* PCR mix - according to standard protocol. | * PCR mix - according to standard protocol. |
Revision as of 13:18, 13 August 2013
12 August 2013
Contents |
lab 208
Main purpose
- Screening PCR on pZA21:RFP araBAD
- PCR reaction in order to amplify backbone pZA21 containing araBAD and RFP
- PCR reaction in order to amplify Nir1 and Nir2 fragments
Who was in the lab
Henrike, Kristian, Gosia, Julia
Procedure
Screening PCR on pZA21:araBAD:RFP spl
8 different conditions and 12 different annealing temperatures were screened.
- PCR mix according to standard protocol with different amounts of water according to the amounts of DMSO and MgCl2 added to the reactions.
The conditions are:
- 1% DMSO + 1uL MgCl2 2mM + GC buffer
- 3% DMSO + 1uL MgCl2 2mM + GC buffer
- 5% DMSO + 1uL MgCl2 2mM + GC buffer
- 5% DMSO + 0.5uL MgCl2 50mM + GC buffer
- 5% DMSO + 2uL MgCl2 50mM + HF buffer
- 3% DMSO + 1uL MgCl2 50mM + HF buffer
- 5% DMSO + 1uL MgCl2 50mM + HF buffer
- 5% DMSO + 1uL MgCl2 2mM + HF buffer
- Primers - 51a and 51b1
- Template - "Ara" sample (plasmid isolation pZA21:araBAD:RFP).
- Annealing temperature: each condition were run in 12 different annealing temperatures with constant interval within the range 51 C-65 C.
PCR mix for backbone
- PCR mix - according to standard protocol.
- Primers - 1an and 1b
- Template - "Ara" sample (plasmid isolation pZA21:araBAD:RFP).
- Program was based on standard program with 65 C of annealing temperature and 4 min of extension time.
- Samples names: 1, 2, 3 and N (negative)
PCR for Nir1 and Nir2
- PCR mix according to standar protocol with changes: addition of DMSO in 3 different final concentrations (2%, 3%, 5%); two different buffers (HF 5x and GC 5x), amount of added water was dependent on volume of added DMSO.
- Primers for Nir1 - 39a, 39b
- Primers for Nir2 - 40a, 40b
- Templates - fragments Nir1 and Nir2 amplified with non-uracil primers, gel purified
- Polymerase x7
- Program (A99 - the same for Nir1 and Nir2) was based on standard PCR program with 50 C and 1 min of annealing parameters and 5 min of extension time.
- Samples names:
- Nir1, GC buffer, 2% DMSO
- Nir1, GC buffer, 3% DMSO
- Nir1, GC buffer, 5% DMSO
- Nir1, HF buffer, 2% DMSO
- Nir1, HF buffer, 3% DMSO
- Nir1, HF buffer, 5% DMSO
- Nir2, GC buffer, 2% DMSO
- Nir2, GC buffer, 3% DMSO
- Nir2, GC buffer, 5% DMSO
- Nir2, HF buffer, 2% DMSO
- Nir2, HF buffer, 3% DMSO
- Nir2, HF buffer, 5% DMSO
Results
Conclusion
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