Imperial College/20 August 2008
From 2008.igem.org
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*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]] | [[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]] | ||
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+ | 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''=== |
Revision as of 22:46, 1 September 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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