Melbourne/Lab Notebook
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*Small number of colonies on BBa_R0084 plate. | *Small number of colonies on BBa_R0084 plate. | ||
*Placed in cool room | *Placed in cool room | ||
+ | |||
+ | ====Transformation==== | ||
+ | #Resuspended the following parts in 15uL: | ||
+ | *BBa_B0034 (RBS, plate 1 3O, Amp) | ||
+ | *BBa_C0051 (C1 repressor, plate 1 5G, Amp) | ||
+ | *BBa_B0010 (Terminator, plate 2 3P, Amp) | ||
+ | **Think some DNA may have remained in wells | ||
+ | #[[Melb:Transformation Protocol|Transformed]] into competent DH5alpha cells from Joe | ||
+ | |||
+ | ====Streak plates==== | ||
+ | #Streaked the following cells: | ||
+ | *PJS010 (from solid agar, Amp) | ||
+ | *Fusion protein (from glycerol stock, Kan) | ||
+ | *BBa_I15010 (from solid agar, Kan) | ||
===27 June 2007=== | ===27 June 2007=== |
Revision as of 01:23, 3 July 2007
Contents |
Week 1
25 June 2007
Prepared LB agar plates.
Transformation
- resuspended the following from Registry plates:
- BBa_I15008 - ho1 (P2 21A)
- BBa_I15009 - PcyA (P2 21C)
- BBa_R0084 - OmpR positive promoter (P1 11H)
- Punctured foil with pipette tip.
- Resuspended in 15uL ddH2O.
- Stored in-20 (after taking 1uL for transformation).
- Transformed into competent DH5alpha cells with shorter incubation times as follows:
- 30min on ice after DNA addition
- 10min on ice after heat shock
- 30min at 37degrees with LB
26 June 2007
Transformation from Monday
- Transformation of BBa_I15008 and BBa_I15009 failed. No colonies on plates
- Small number of colonies on BBa_R0084 plate.
- Placed in cool room
Transformation
- Resuspended the following parts in 15uL:
- BBa_B0034 (RBS, plate 1 3O, Amp)
- BBa_C0051 (C1 repressor, plate 1 5G, Amp)
- BBa_B0010 (Terminator, plate 2 3P, Amp)
- Think some DNA may have remained in wells
- Transformed into competent DH5alpha cells from Joe
Streak plates
- Streaked the following cells:
- PJS010 (from solid agar, Amp)
- Fusion protein (from glycerol stock, Kan)
- BBa_I15010 (from solid agar, Kan)