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Team:DTU-Denmark/Notebook/9 July 2013
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| - | =208= | + | {{:Team:DTU-Denmark/Templates/StartPage|9 July 2013}} |
| + | Navigate to the [[Team:DTU-Denmark/Notebook/8_July_2013|Previous]] or the [[Team:DTU-Denmark/Notebook/10_July_2013|Next]] Entry | ||
| + | =Lab 208= | ||
| + | <hr/> | ||
==Main purpose== | ==Main purpose== | ||
| + | <hr/> | ||
Run gel with 7 PCR samples of Nir operon from ''Pseudomonas aeruginosa'' and purified AMO, HAO and CYC from 08.07.2013. | Run gel with 7 PCR samples of Nir operon from ''Pseudomonas aeruginosa'' and purified AMO, HAO and CYC from 08.07.2013. | ||
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==Who was in the lab== | ==Who was in the lab== | ||
| - | Ariadni,Henrike,Julia,Gosia | + | <hr/> |
| + | Ariadni, Henrike, Julia, Gosia | ||
==Procedure== | ==Procedure== | ||
| - | + | <hr/> | |
===Run gel=== | ===Run gel=== | ||
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===Extraction PCR=== | ===Extraction PCR=== | ||
| + | to produce the right fragment of the Nir operon from either chromosomal DNA from ''Pseudomonas aeruginosa'' or the too long PCR fragments from the 08.07. | ||
| + | |||
6 samples | 6 samples | ||
| + | |||
*3 samples from culture pAO1 | *3 samples from culture pAO1 | ||
| - | *3 samples from | + | *3 samples from today's purification of the PCR that was done on 08.07. |
| - | 7 reactions | + | master mix for 7 reactions |
* dNTP: 1 ul (7 ul) | * dNTP: 1 ul (7 ul) | ||
* HF buffer: 10 ul (70 ul) | * HF buffer: 10 ul (70 ul) | ||
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Settings for PCR | Settings for PCR | ||
| - | {| class="wikitable | + | {| class="wikitable" style="text-align: right" |
! Temperature (<sup>o</sup>C)!! Time (min)!! Rounds | ! Temperature (<sup>o</sup>C)!! Time (min)!! Rounds | ||
|- | |- | ||
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==Results== | ==Results== | ||
| + | <hr/> | ||
Nanodrop measurement of Nir operon: | Nanodrop measurement of Nir operon: | ||
* 17.98 ng/ul | * 17.98 ng/ul | ||
* 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}} | ||
Latest revision as of 20:39, 16 September 2013
9 July 2013
Contents |
Lab 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
to produce the right fragment of the Nir operon from either chromosomal DNA from Pseudomonas aeruginosa or the too long PCR fragments from the 08.07.
6 samples
- 3 samples from culture pAO1
- 3 samples from today's purification of the PCR that was done on 08.07.
master mix for 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
