IGEM:Harvard/2008/Lab Notebooks/DailyBook/Week1: Difference between revisions

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| align="center" style="background:#eeeeee;"|'''Size'''
| align="center" style="background:#eeeeee;"|'''Size'''
| align="center" style="background:#eeeeee;"|'''Marker'''
| align="center" style="background:#eeeeee;"|'''Marker'''
| align="center" style="background:#eeeeee;"|
| align="center" style="background:#eeeeee;"|'''Number of Colonies'''
|-
|-
| [http://partsregistry.org/Part:BBa_M30109 P11]||Light responsive system, dual regulation||pUC19-derived pMB1||4333||Amp/Cm
| [http://partsregistry.org/Part:BBa_M30109 P11]||Light responsive system, dual regulation||pUC19-derived pMB1||4333||Amp/Cm||224
|-
|-
| [http://partsregistry.org/Part:BBa_I13522 P15]||GFP with Tet promoter||ColE1||937||Amp
| [http://partsregistry.org/Part:BBa_I13522 P15]||GFP with Tet promoter||ColE1||937||Amp||360
|-
|-
| [http://partsregistry.org/Part:BBa_R0040 P16]||Tet repressible promoter||pMB1||54||Amp
| [http://partsregistry.org/Part:BBa_R0040 P16]||Tet repressible promoter||pMB1||54||Amp||264
|-
|-
| [http://partsregistry.org/Part:BBa_Q04400 P17]||Inverter (TetR w/o promoter and Tet promoter)||OriS, P1 lytic, F1||902||Kan
| [http://partsregistry.org/Part:BBa_Q04400 P17]||Inverter (TetR w/o promoter and Tet promoter)||OriS, P1 lytic, F1||902||Kan||2
|-
|-
| [http://partsregistry.org/Part:BBa_R0051 P18]||lambda promoter (cI regulated)||pMB1||49||Amp
| [http://partsregistry.org/Part:BBa_R0051 P18]||lambda promoter (cI regulated)||pMB1||49||Amp||112
|-
|-
| [http://partsregistry.org/Part:BBa_I763007 P19]||RFP with lambda promoter||pMB1||918||Amp
| [http://partsregistry.org/Part:BBa_I763007 P19]||RFP with lambda promoter||pMB1||918||Amp||104
|-
|-
| [http://partsregistry.org/Part:BBa_J04431 P20]||GFP (LVA tagged) with Lac promoter||pMB1||1122||Amp, Kan
| [http://partsregistry.org/Part:BBa_J04431 P20]||GFP (LVA tagged) with Lac promoter||pMB1||1122||Amp, Kan||136
|}
|}



Revision as of 12:01, 23 June 2008

Monday: June 23, 2008

Chemical

Results from Friday (6/20) Electroporation and Transformation in S1

Name Registry Name Description Origin Marker Observations
P1a J23113 Low promoter GFP tester pMB1 Kan 16 pink colonies of approx 7mm diameter
P2a J23150 Medium promoter GFP tester pMB1 Kan no growth
P3a J23151 High promoter GFP tester pMB1 Kan 8 pink colonies of approx 7mm diameter
P12 pETDuet-1 Low copy plasmid pBR322-derived ColE1 Amp Lawn
P13 pCDFDuet-1 Low copy plasmid CloDF13 Sm 41 pink colonies and some small yellow ones that may be E. coli
P14 pCOLADuet-1 Low copy plasmid ColA Kan No growth

Light

Transformations of P11, P15-20

Name Description Origin Size Marker Number of Colonies
P11 Light responsive system, dual regulation pUC19-derived pMB1 4333 Amp/Cm 224
P15 GFP with Tet promoter ColE1 937 Amp 360
P16 Tet repressible promoter pMB1 54 Amp 264
P17 Inverter (TetR w/o promoter and Tet promoter) OriS, P1 lytic, F1 902 Kan 2
P18 lambda promoter (cI regulated) pMB1 49 Amp 112
P19 RFP with lambda promoter pMB1 918 Amp 104
P20 GFP (LVA tagged) with Lac promoter pMB1 1122 Amp, Kan 136

Restreaking

6/23: P16, which has GFP under a constitutive Tet promoter did not appear to fluoresce, so we restreaked all the of the plates (with the same antibiotic on which they were originally grown). They were left in the 37 degree incubator along with a blank Kan and a blank Amp plate (- controls).

Overnight cultures

6/23: The above was repeated in 5mL LB liquid cultures instead of plates.

Widgetry


Tuesday: June 24, 2008


Wednesday: June 25, 2008


Thursday: June 26, 2008


Friday: June 27, 2008