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Team:Groningen/Labwork/24 July 2013
From 2013.igem.org
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<h2>Claudio</h2> | <h2>Claudio</h2> | ||
| - | <br>The plates are taken out | + | <br>The plates are taken out from the incubator and the presence of RFP is detected using UV light.</br> |
| - | <img src=" | + | <img src="https://2013.igem.org/File:Munich_woIPTG.jpg" alt="Plate1" width="40%" > |
<br><b>PICUTRES</b></br> | <br><b>PICUTRES</b></br> | ||
Revision as of 12:20, 24 July 2013
Mirjam
Run the samples of the PCR made 23-07 over a 1.5% agarose gel. The samples show the presence of the expected bands for 3 out of 4 signal sequences. So it is tried to obtain these samples by Gel extraction. No bands are seen on gel. Made a restriction digestion of the rest of the samples of silk 2 and 3 (strepF-R and F-strepR) to obtain a higher concentration. With the restriction digest a ligation to the four signal sequences is made. The primers that are ordered for heat motility are found and diluted. A PCR is made to obtain Pdes, CheY RBS.
Inne
Made a -80 stock of the Munich BBa_k823023 backbone + our IPTG promoter.
Made a miniprep of the inoculated cells with the k077557 biobrick that Chicago requested.
Concentration of the final sample is 21.1 ng/uL.
Sample was stored in -20 freezer.
Claudio
The plates are taken out from the incubator and the presence of RFP is detected using UV light.
PICUTRES
