User contributions
- 02:44, 4 October 2012 (diff | hist) . . (-13) . . Part:BBa K880001 (current)
- 02:44, 4 October 2012 (diff | hist) . . (+39) . . Part:BBa K880001
- 01:47, 4 October 2012 (diff | hist) . . (+44) . . Part:BBa K880002 (current)
- 01:45, 4 October 2012 (diff | hist) . . (+392) . . Part:BBa K880005
- 01:38, 4 October 2012 (diff | hist) . . (+1,505) . . Part:BBa K880003 (current)
- 01:38, 4 October 2012 (diff | hist) . . (0) . . N File:MichFig6.png (current)
- 01:36, 4 October 2012 (diff | hist) . . (0) . . N File:MichFig5.png (current)
- 01:34, 4 October 2012 (diff | hist) . . (+1,786) . . Part:BBa K880002
- 01:24, 4 October 2012 (diff | hist) . . (-1) . . Part:BBa K880001
- 01:24, 4 October 2012 (diff | hist) . . (+2,538) . . Part:BBa K880001
- 01:23, 4 October 2012 (diff | hist) . . (0) . . N File:MichFig8.jpg (current)
- 01:23, 4 October 2012 (diff | hist) . . (0) . . N File:MichFig7.png (current)
- 01:16, 4 October 2012 (diff | hist) . . (0) . . Part:BBa K880000
- 01:15, 4 October 2012 (diff | hist) . . (-50) . . m Part:BBa K880000
- 01:11, 4 October 2012 (diff | hist) . . (+278) . . Part:BBa K880000
- 01:09, 4 October 2012 (diff | hist) . . (-17) . . Part:BBa K880000
- 01:09, 4 October 2012 (diff | hist) . . (-279) . . Part:BBa K880000
- 01:08, 4 October 2012 (diff | hist) . . (0) . . N File:MichFig9.png (current)
- 01:08, 4 October 2012 (diff | hist) . . (-4) . . Part:BBa K880000
- 01:08, 4 October 2012 (diff | hist) . . (+1,080) . . Part:BBa K880000
- 21:27, 30 September 2012 (diff | hist) . . (+102) . . Part:BBa K880004
- 21:27, 30 September 2012 (diff | hist) . . (+102) . . Part:BBa K880003
- 21:26, 30 September 2012 (diff | hist) . . (+102) . . Part:BBa K880002
- 21:26, 30 September 2012 (diff | hist) . . (+102) . . Part:BBa K880001
- 21:24, 30 September 2012 (diff | hist) . . (+101) . . Part:BBa K880000
- 18:55, 30 September 2012 (diff | hist) . . (+413) . . N Part:BBa K880004 (New page: =='''LVA Tag in RFC25'''== The amino acid sequence AANDENYALVA can be fused onto proteins in order to rapidly reduce their half life in the cytoplasm. Responsiveness for genetic circuits ...)
- 18:54, 30 September 2012 (diff | hist) . . (+348) . . N Part:BBa K880003 (New page: =='''A Utility for Assaying fim-Based Recombinases'''== -IRL K137010 + Sequence with AgeI cut-site K165006 + IRR K137008 Mi8 This is an asymmetrically digestible reporter, same orientati...)
- 18:53, 30 September 2012 (diff | hist) . . (+66) . . Part:BBa K880002
- 18:52, 30 September 2012 (diff | hist) . . (+927) . . N Part:BBa K880002 (New page: -IRR K137008 + inverted tetR promoter K137047 + IRL K137010 + GFP I13504 (MI275) -GFP fluorescence reporter to assay the activity of FimE K137007 and HbiF K880000 recombinases. This ha...)
- 18:50, 30 September 2012 (diff | hist) . . (-2) . . Part:BBa K880001 (→A Utility for Assaying fim-Based Recombinases)
- 18:16, 30 September 2012 (diff | hist) . . (+853) . . N Part:BBa K880001 (New page: =='''A Utility for Assaying fim-Based Recombinases'''== K880001 is a utility for characterizing the functionality of fim based recombinases such as FimB, FimE, and HbiF and consists of K1...)
- 17:50, 30 September 2012 (diff | hist) . . (+34) . . Part:BBa K880000
- 17:47, 30 September 2012 (diff | hist) . . (+1,710) . . N Part:BBa K880000 (New page: The Hbif recombinase is a putative regulator of the Escherichia coli type 1 fimbriation system, capable of switching the fimS invertible region in the production of fimbriae in a manner si...)