Team:DTU-Denmark/Notebook/12 August 2013
From 2013.igem.org
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 adjusted amounts of water according to the amounts of DMSO and MgCl2 added to the reactions.
The conditions are:
Row | DMSO | MgCl2 | buffer |
---|---|---|---|
A | 1% | 0.04mM | GC |
B | 3% | 0.04mM | GC |
C | 5% | 0.04mM | GC |
D | 5% | 0.5mM | GC |
E | 5% | 2mM | GC |
F | 3% | 1mM | HF |
G | 5% | 1mM | HF |
H | 5% | 0.04mM | HF |
- Primers - 51a and 51b1
- Template - "Ara" sample (plasmid isolation pZA21:araBAD:RFP).
- Annealing temperature: each condition were run in the following 12 different annealing temperatures:
- 53.2 C
- 53.5 C
- 54.6 C
- 56 C
- 57.2 C
- 58.4 C
- 59.6 C
- 60.6 C
- 61.9 C
- 63.2 C
- 64.6 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 standard 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
See gels on tomorrow's page.
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