Melbourne/Lab Notebook
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====Miniprep==== | ====Miniprep==== | ||
*miniprepped the following overnight cultures set up on the 4th of July | *miniprepped the following overnight cultures set up on the 4th of July | ||
| - | ** | + | **[[Melbourne/BBa_B0010|'''P2 3P 1''']] |
| + | **[[Melbourne/BBa_B0010|'''P2 3P 2''']] | ||
| + | **[[Melbourne/BBa_I15010|'''I15010 1''']] | ||
| + | **[[Melbourne/BBa_I15010|'''I15010 2''']] | ||
| + | **[[Melbourne/pJS010|'''pJS010 1''']] | ||
| + | **[[Melbourne/pJS010|'''pJS010 2''']] | ||
| + | **[[Melbourne/Fusion|'''Fusion 1''']] | ||
| + | **[[Melbourne/Fusion|'''Fusion 2''']] | ||
| + | **[[Melbourne/BBa_J61035|'''P4 8J 1''']] | ||
| + | **[[Melbourne/BBa_J61035|'''P4 8J 2''']] | ||
| + | **[[Melbourne/BBa_E0241|'''P2 15L 1''']] | ||
| + | **[[Melbourne/BBa_E0241|'''P2 15L 2''']] | ||
| + | **[[Melbourne/BBa_Q04510|'''P2 13K 1''']] | ||
| + | **[[Melbourne/BBa_Q04510|'''P2 13K 2''']] | ||
| + | **[[Melbourne/BBa_B0014|'''P1 1G 1''']] | ||
| + | **[[Melbourne/BBa_B0014|'''P1 1G 2''']] | ||
| + | *the following liquid cultures were not miniprepped due to failure (no growth) | ||
| + | **[[Melbourne/BBa_R0084|'''P1 11H 1''']] | ||
| + | **[[Melbourne/BBa_R0084|'''P1 11H 2''']] | ||
| + | **[[Melbourne/BBa_E0040|'''P1 5H 1''']] | ||
| + | **[[Melbourne/BBa_E0040|'''P1 5H 2''']] | ||
| + | **suspected contaminating colony from [[Melbourne/BBa_J61035|'''P4 8J''']] | ||
===6 July 2007=== | ===6 July 2007=== | ||
Revision as of 02:18, 5 July 2007
Contents |
Week 1
25 June 2007
Prepared LB agar plates.
Transformation
- resuspended the following from Registry plates:
- 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:
- 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
- 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:
- 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:
- Stored in -20 freezer
Digest
Liquid culture
- Cultured the following cells from transformed plates:
29 June 2007
Miniprep
- Minipreped the cultures grown overnight after putting aside 1mL(sterile) for glycerol stocks:
- Stored in -20 freezer
30 June 2007
Week 2
2 July 2007
Now
3 July 2007
4 July 2007
Ampicillin Plates
- Made up 25 Ampicillin plates using 400mL LB agar prepared on the 25th of June.
- Used 100mg/ml Ampicillin stock from Gooley Lab - In bag in left freezer near our lab bench.
5 July 2007
Miniprep
- miniprepped the following overnight cultures set up on the 4th of July
- the following liquid cultures were not miniprepped due to failure (no growth)
