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Team:TUDelft/3 August 2009
From 2009.igem.org
Lab Notebook
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3 August 2009
Calin
Tim pointed out that the plasmids should be linearized before doing the gel. Here are possible digestions on some of the parts:
| Backbone | Part | Unique Sites Present |
| pSB1A2 | oriT-R | AatII
AccI AflIII BglI BspLU11I BstAPI DrdI Eam1105I EcoRI FspI NspI PstI PvuI RsaI ScaI SgrAI SpeI SspI StyI TatI VspI XbaI XmnI ZraI |
| BBa_J61002 | strong promoter | AatII
AlwNI AvrII BglI BsiWI
BspLU11I BstXI DrdI EcoRI FspI HaeII HpaI NcoI NspI PflMI PshAI PstI PvuI PvuII RsrII ScaI SgrAI SpeI SspI TatI VspI XbaI XmnI ZraI |
| pSB1AK3 | ccdB | AatII
AccB1I AccI BamHI BanII BglI BspLU11I BsrGI BssHII BstXI BstZ17I BtrI ClaI DraIII DrdI Eam1105I EcoNI EcoRI FspI HaeII HincII HindIII MscI NruI NspI PflMI PstI ScaI SgfI SpeI SrfI XbaI XmnI ZraI |
| pSB4C5 | ccdB | AatII
AccI AclI AflII ApaLI BamHI BbeI BseRI BsrGI BssHII BstAPI BstXI BstZ17I BtrI Cfr10I EcoRI EcoRV HaeII HincII KasI NarI NdeI PstI PvuII SacI ScaI SfoI SmaI SpeI SphI SrfI StyI XbaI XmaI ZraI |
Growth on all plates. The pSB4C5 plate was parafilmed and placed in fridge.
