Team:DTU-Denmark/Notebook/27 August 2013
From 2013.igem.org
27 August 2013
Contents |
lab 208
Main purpose
Who was in the lab
Procedure
PCR reactions
compound | amount (in uL) | |
---|---|---|
standard mix | additive mix | |
dNTPs | 1 | 1 |
X7 ploymerase | 0.5 | 0.5 |
HF buffer | 10 | 10 |
MilliQ | 18 uL | |
FW primer | 3 uL | |
RV primer | 3 uL | |
template | 1 uL | |
DMSO | - | 2.5 |
50 mM MgCl2 | - | 2 |
Template was made by resuspending 1 culture in 100uL MilliQ.
program:
temperature | time | cycles |
---|---|---|
98C | 10:00 | - |
98C | 0:10 | 36 |
annealing temperature | 0:30 | 36 |
72C | 0:20 | 36 |
72C | 5:00 | - |
10C | hold | - |
Results
Gel
- 1 kb ladder
- pSB1C3 for Biobricks, HF buffer
- pSB1C3 for Biobricks, HF buffer, 5%DMSO
- pSB1C3 for Biobricks, GC buffer
- pSB1C3 for Biobricks, GC buffer, 5%DMSO
- negative pSB1C3 for Biobricks
- pZA21::ara for USER ligation with Nir
- pZA21::ara for USER ligation with Nir (duplicate)
- 1 kb ladder
Note: It seems the ladder overflew.
Conclusion
Navigate to the Previous or the Next Entry