Imperial College/4 September 2008
From 2008.igem.org
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As can be seen, both the AmyE 3' integration sequence and the Aad9 (spectinomycin resistance) gene amplified properly. LacI did not however and so this will need to be repeated. | As can be seen, both the AmyE 3' integration sequence and the Aad9 (spectinomycin resistance) gene amplified properly. LacI did not however and so this will need to be repeated. | ||
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+ | ==Dry Lab== | ||
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+ | ===Motility=== | ||
+ | *Tested Volocity software on 64-Bit analysis computer in SAF (FILM facility). Visually, volocity tracks cells very well, including synthetic data with a single motile ellipse without any change in shape. However, the software is unable to continuously track synthetic data of multiple ellipses with changing shape. It loses track of the cells after a few frames. When tested on real data, it tracks cells which run for fairly long, but it does not track tumbling cells. Most tracks do not last over 30 frames, which is considerable little for any form of good data to be extracted. | ||
+ | *Hence we are still pursuing manual tracking, but if time permits, we will attempt to use other forms of filtering to achieve the best form of tracking for Volocity. | ||
+ | *Error bars were plotted for Volocity software and uploaded onto the OWW wiki. |
Revision as of 18:08, 5 September 2008
4 September 2008WetlabCloning
Preparation of Electrocompetent E. coli CellsWe have prepared 42 aliquots of electrocompetent XL1 Blue E. coli cells using [http://openwetware.org/wiki/IGEM:IMPERIAL/2008/New/Protocols/XL1-Blue_preparation the relevant protocol] listed on our Protocols Page. The protocol was updated to include a higher innoculation value from the overnight culture. ResultsAs can be seen, both the AmyE 3' integration sequence and the Aad9 (spectinomycin resistance) gene amplified properly. LacI did not however and so this will need to be repeated.
Dry LabMotility
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