User contributions
From 2008.igem.org
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- 13:53, 7 August 2008 (diff | hist) Virginia/6 August 2008 (top)
- 14:47, 6 August 2008 (diff | hist) N Virginia/6 August 2008 (New page: ==TODO== *Miniprep the new overnight broths of the assemblies trying to redo the *Digest the miniprepped DNA *Gel the digested DNA *If bands come up as expected, run a nusieve gel to extr...)
- 14:38, 6 August 2008 (diff | hist) Virginia/4 August 2008 (→Accomplished) (top)
- 14:37, 6 August 2008 (diff | hist) N Virginia/5 August 2008 (New page: ==TODO== *Re-gel the digested parts to cut out parts and carry on with the second stage of assemblies ==Results== *second running of gel did not show any different results. Some digested ...) (top)
- 13:55, 6 August 2008 (diff | hist) N Virginia/4 August 2008 (New page: ==Goals== *Assemblies 51-57 **Digest for standard assembly **Use low melt gel to purify parts ==Accomplished== *Gel of assemblies not as expected **Potential bands of small cutouts not vi...)
- 13:48, 6 August 2008 (diff | hist) N Virginia/1 August 2008 (New page: ==Goals== *Assemblies 46-50 **Plan to use low melt gel to separate parts **Standard assembly ==Accomplished== *Difficulties with the low-melt gel **Bands are crooked, not the right length...) (top)
- 19:27, 28 July 2008 (diff | hist) Team:Virginia/Protocols
- 21:34, 22 July 2008 (diff | hist) m Team:Virginia/Protocols (→Electrophoresis Gel (Making))
- 21:33, 22 July 2008 (diff | hist) Team:Virginia/Protocols (→3A assembly Ligation)
- 20:36, 22 July 2008 (diff | hist) Team:Virginia/Protocols (→Gel Electrophoresis (Loading & Running))
- 20:52, 21 July 2008 (diff | hist) Team:Virginia/Protocols (→Electrophoresis Gel)
- 20:26, 21 July 2008 (diff | hist) Team:Virginia/Protocols (→Electrophoresis Gel)
- 18:03, 21 July 2008 (diff | hist) m Virginia/21 July 2008 (top)
- 18:02, 21 July 2008 (diff | hist) m Virginia/21 July 2008 (→Where We Stand)
- 18:00, 21 July 2008 (diff | hist) Virginia/21 July 2008
- 17:49, 21 July 2008 (diff | hist) N Virginia/21 July 2008 (New page: ==Where We Stand== *'''Genetic Attenuator''' *Measurement Plasmid **Activating Promoter with Arabinos X'''incomplete''' **Suspicion that measurement plasmid may not work in DB3.1 cells we...)
- 17:26, 21 July 2008 (diff | hist) m Virginia/19 July 2008 (top)
- 15:00, 18 July 2008 (diff | hist) Team:Virginia/Protocols (→Electrophoresis Gel)
- 14:48, 18 July 2008 (diff | hist) Team:Virginia/Protocols
- 14:38, 18 July 2008 (diff | hist) Nm Team:Virginia/Protocols (New page: Hello World)
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