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Team:Groningen/Labwork/26 June 2013
From 2013.igem.org
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| - | <br>The PCR product is loaded on gel to examine if the PCR reaction succeeded. | + | <br>The PCR product is loaded on <a href="https://2013.igem.org/Team:Groningen/protocols/GelElectrophoresis"><FONT COLOR="black"><b>gel</b></FONT></a> to examine if the PCR reaction succeeded. |
<br>picture | <br>picture | ||
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<h2>Claudio and Inne</h2> | <h2>Claudio and Inne</h2> | ||
Further discussion about the available options to create a heat-attracted bacteria. | Further discussion about the available options to create a heat-attracted bacteria. | ||
Latest revision as of 16:17, 28 July 2013
Mirjam
Did a genomic DNA extraction of B. subtilis strain 168. Two tubes are obtained from this with a concentration of 66ng/µl and 67ng/µl.The primers for our main subject, silk secretion, arrived. The primers are diluted to a concentration of 10mM.
To run a PCR, dNTPs are necessary in a concentration of 10mM, so this dilution is also made.
A PCR reaction mix is made for the four different signal sequences.
| signal sequence | Tm-5 | size |
|---|---|---|
| FliZ | 45°C | 130 |
| MotB | 50°C | 100-150 |
| EstA | 50°C | 100-150 |
| LytB | 50°C | 100-150 |
The PCR product is loaded on gel to examine if the PCR reaction succeeded.
picture
