Imperial College/20 August 2008
From 2008.igem.org
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|{{#calendar: title=Imperial_College |year=2008 | month=08}} | |{{#calendar: title=Imperial_College |year=2008 | month=08}} | ||
|{{#calendar: title=Imperial_College |year=2008 | month=09}} | |{{#calendar: title=Imperial_College |year=2008 | month=09}} | ||
- | | rowspan="2" bgcolor=# | + | | rowspan="2" bgcolor=#ffffff width="100%" | |
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= 20 August 2008 = | = 20 August 2008 = | ||
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*GFP-3-mutB - Terminator and CAT overnight cultures miniprepped (all 3ml). | *GFP-3-mutB - Terminator and CAT overnight cultures miniprepped (all 3ml). | ||
- | *Single digests (''EcoRI'') of all registry sequences performed and assayed by gel to check vector size | + | *Single digests (''EcoRI'') of all registry sequences performed and assayed by gel to check vector size |
+ | [[Image:20-8.PNG|center|frame| All run DNA was digested with ''EcoRI'' to linearise for optimal running. Lanes : M = Marker, 1 = Terminator Mini 1 , 2 = Terminator Mini 2, 3 = Terminator Mini 3, 4 = mRFP - terminator Mini 1 , 5 = mRFP - terminator Mini 2, 6 = mRFP - terminator Mini 3, 7 = AK3 Mini 1 , 8 = AK3 Mini 2, 9 = AK3 Mini 3, 10 = GFP-mut3b - terminator Mini 1 , 11 = GFP-mut3b - terminator Mini 2, 12 = GFP-mut3b - terminator Mini 3, 13 = CAT Mini 1 , 14 = CAT Mini 2, 15 = CAT Mini 3]] | ||
+ | |||
+ | All major bands correspond to the approximate size of vector and insert. In several of the minis a second band is however visible is most likely to be denatured DNA as a byproduct of doing all the minipreps in one go (and so taking too long) | ||
===''B.subtilis''=== | ===''B.subtilis''=== | ||
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==Dry Lab== | ==Dry Lab== | ||
- | * About to complete | + | * About to complete Tutorial 2 |
* Preliminary work on validating the tracking algorithm written by EPFL using video generated from synthetic data | * Preliminary work on validating the tracking algorithm written by EPFL using video generated from synthetic data | ||
* Preliminary work on growth curve of Bacillus Subtilis | * Preliminary work on growth curve of Bacillus Subtilis | ||
- | * We are aiming to produce a chassis characterisation | + | * We are aiming to produce a chassis characterisation. |
+ | <br> | ||
+ | {{Imperial/EndPage|Notebook|Notebook}} |
Latest revision as of 20:38, 28 October 2008
20 August 2008Wet LabCloning
All major bands correspond to the approximate size of vector and insert. In several of the minis a second band is however visible is most likely to be denatured DNA as a byproduct of doing all the minipreps in one go (and so taking too long) B.subtilis
Dry Lab
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