"
Team:DTU-Denmark/Notebook/9 July 2013
From 2013.igem.org
(Difference between revisions)
(→Who was in the lab) |
|||
| Line 1: | Line 1: | ||
| + | {{:Team:DTU-Denmark/Templates/StartPage|}} | ||
| + | |||
=208= | =208= | ||
==Main purpose== | ==Main purpose== | ||
| Line 48: | Line 50: | ||
* 16.82 ng/ul | * 16.82 ng/ul | ||
* 8.51 ng/ul | * 8.51 ng/ul | ||
| + | |||
| + | Navigate to the [[Team:DTU-Denmark/Notebook/8_July_2013|Previous]] or the [[Team:DTU-Denmark/Notebook/10_July_2013|Next]] Entry | ||
| + | |||
| + | {{:Team:DTU-Denmark/Templates/EndPage}} | ||
Revision as of 16:37, 16 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
6 samples
- 3 samples from culture pAO1
- 3 samples from PCR purification of 08.07
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)
Settings for PCR
| Temperature (oC) | Time (min) | Rounds |
|---|---|---|
| 98 | 2:00 | 1 |
| 98 | 0:20 | 35 |
| 66 | 0:45 | 35 |
| 72 | 9:00 | 35 |
| 72 | 5:00 | 1 |
| 4 | ∞ | - |
Results
Nanodrop measurement of Nir operon:
- 17.98 ng/ul
- 16.82 ng/ul
- 8.51 ng/ul
Navigate to the Previous or the Next Entry
