Melbourne/Lab Notebook
From 2007.igem.org
(Difference between revisions)
m (Melb:Lab Notebook moved to Melbourne/Lab Notebook) |
(→Transformation) |
||
Line 8: | Line 8: | ||
#resuspended the following from Registry plates: | #resuspended the following from Registry plates: | ||
#*[[Melb:BBa_I15008|'''P2 21A''']] - (BBa_I15008, ho1, Kan) | #*[[Melb:BBa_I15008|'''P2 21A''']] - (BBa_I15008, ho1, Kan) | ||
- | #*'''P2 21C''' - (BBa_I15009, PcyA, Kan) | + | #*[[Melbourne/BBa_I15009|'''P2 21C''' - (BBa_I15009, PcyA, Kan) |
- | #*'''P1 11H''' - (BBa_R0084, OmpR positive promoter, Amp) | + | #*[[Melbourne/BBa_R0084]]'''P1 11H''' - (BBa_R0084, OmpR positive promoter, Amp) |
#Punctured foil with pipette tip. | #Punctured foil with pipette tip. | ||
#Resuspended in 15uL ddH2O. | #Resuspended in 15uL ddH2O. |
Revision as of 00:29, 4 July 2007
Contents |
Week 1
25 June 2007
Prepared LB agar plates.
Transformation
- resuspended the following from Registry plates:
- P2 21A - (BBa_I15008, ho1, Kan)
- [[Melbourne/BBa_I15009|P2 21C - (BBa_I15009, PcyA, Kan)
- Melbourne/BBa_R0084P1 11H - (BBa_R0084, OmpR positive promoter, Amp)
- 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, P1 3O, Amp)
- BBa_C0051 (C1 repressor, P1 5G, Amp)
- BBa_B0010 (Terminator, P2 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, Amp?)
- BBa_I15010 (from solid agar, Kan)
27 June 2007
Transformation
- Repeated transformation of failed parts from Monday:
- BBa_I15008 (Kan)
- BBa_I15009 (Kan)
- Used resuspended DNA that was stored on Monday
Liquid culture
- Prepared 30mL of Amp LB (100ug/mL). Prepared 5mL Kan LB (50mg/mL).
- Aliquoted 5mL Amp LB into 6 50mL falcon tubes
- To the Amp LB aliquots single transformed colonies from plates of the following were introduced:
- PJS010
- Fusion
- BBa_B0034
- BBa_C0051
- BBa_B0010
- BBa_R0084
- To the Kan LB a single colony from the transformation plate of BBa_I15010 was introduced.
- Cells incubated at 37degrees with shaking overnight.
28 June 2007
Miniprep
- Minipreped the cultures grown overnight after putting aside 1mL(sterile) for glycerol stocks:
- PJS010
- Fusion
- BBa_B0034
- BBa_C0051
- BBa_B0010
- BBa_R0084
- BBa_I15010
- Stored in -20 freezer
Digest
Liquid culture
- Cultured the following cells from transformed plates:
- BBa_R0084
- BBa_I15010
- BBa_B0034
- BBa_C0051
- BBa_I15008
- BBa_I15009
29 June 2007
Miniprep
- Minipreped the cultures grown overnight after putting aside 1mL(sterile) for glycerol stocks:
- BBa_R0084
- BBa_I15010
- BBa_B0034
- BBa_C0051
- BBa_I15008
- BBa_I15009
- Stored in -20 freezer