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Team:DTU-Denmark/Notebook/9 July 2013
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===Purification of Nir DNA according to the protocol QIA purification protocol. (given in the Kit)=== | ===Purification of Nir DNA according to the protocol QIA purification protocol. (given in the Kit)=== | ||
| - | ===PCR=== | + | ===Extraction PCR=== |
| + | 7 reactions | ||
| + | * dNTP: 1 ul (7 ul) | ||
| + | * HF buffer: 10 ul (70 ul) | ||
| + | * Phusion polymerase: 0.5 ul (3.5 ul) | ||
| + | * H<sub>2</sub>O: 31.5 ul (220.5 ul) | ||
==Results== | ==Results== | ||
Revision as of 08:26, 10 July 2013
Contents |
208
Main purpose
Run gel with 7 PCR samples of Nir operon from Pseudomonas aeruginosa and purified AMO, HAO and CYC from 08.07.2013.
Purification of Nir operon and Nanodrop measurement.
Set up new PCR reaction to extract Nir from Pseudomonas aeruginosa.
Who was in the lab
Ariadni,Henrike,Julia,Gosia
Procedure
Run gel
Purification of Nir DNA according to the protocol QIA purification protocol. (given in the Kit)
Extraction PCR
7 reactions
- dNTP: 1 ul (7 ul)
- HF buffer: 10 ul (70 ul)
- Phusion polymerase: 0.5 ul (3.5 ul)
- H2O: 31.5 ul (220.5 ul)
Results
Nanodrop measurement of Nir operon:
- 17.98 ng/ul
- 16.82 ng/ul
- 8.51 ng/ul
