Team:TUDelft/3 August 2009

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Lab Notebook

July
MTWTFSS
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6 7 8 9 10 11 12
13 14 15 16 17 18 19
20 21 22 23 24 25 26
27 28 29 30 31
August
MTWTFSS
          1 2
3 4 5 6 7 8 9
10 11 12 13 14 15 16
17 18 19 20 21 22 23
24 25 26 27 28 29 30
31
September
MTWTFSS
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7 8 9 10 11 12 13
14 15 16 17 18 19 20
21 22 23 24 25 26 27
28 29 30
October
MTWTFSS
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5 6 7 8 9 10 11
12 13 14 15 16 17 18
19 20 21 22 23 24 25
26 27 28 29 30 31
 

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.