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Team:Cornell/Notebook/Salicylate reporter
From 2012.igem.org
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* Took PCR out of thermal cycler at 9:00 am (DPW) | * Took PCR out of thermal cycler at 9:00 am (DPW) | ||
** Set up gel using NEB 100bp and 2-log ladders (10:00am) | ** Set up gel using NEB 100bp and 2-log ladders (10:00am) | ||
| + | <br> | ||
* Continued gel extraction of p21 PCR digest from previous day (SS) | * Continued gel extraction of p21 PCR digest from previous day (SS) | ||
* Set up ligation of p21 PCR digest extraction and dephosphorylated pBBRBB+mtrB (11:11am, SS) | * Set up ligation of p21 PCR digest extraction and dephosphorylated pBBRBB+mtrB (11:11am, SS) | ||
| + | ** Desalted ligation using Millipore membrane paper | ||
| + | ** Transformed 2 electrocompetent DH5alpha stocks at 5:30 pm and 5:50 pm, respectively. | ||
| + | ** Observed time constants for electroporation of 4.38 ms and 4.24 ms, respectively | ||
| + | ** Let cells recover for 1 hour, plated on LB + Kan. | ||
| + | <br> | ||
| + | * Set up two ligations of pSB3C5 into [PNNL] electrocompetent Shewanella strain JG700 (6:30 pm, Sp.C and St.C) | ||
| + | ** First transformation performed at usual PNNL voltage of 0.75 kV (time constant of 9.30 ms) | ||
| + | ** Second transformation performed at [Myers and Myers] specification of 0.55 kV. | ||
Revision as of 22:51, 30 June 2012
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June
Week
June 29th, Friday
- Vent PCR at 11:00 (DPW)
- Amplifying both previous Phusion PCR band and original p21 template
- Dylan's magic triple anneal method (55/60/63)
- Gel purified PCR product from Phusion template (~1:20 pm) (DPW)
- Quantified product at 22.4 ng/uL
- Set up digestion of p21 PCR product with EcoRI-HF and AscI (~9:00 pm).
- 22 ng/uL --> 45.5 uL sample for 1 ug digest
- Buffer 4
- Ran digestion on gel. (~11:00 pm)
- Sliced out relevant band on gel, stored overnight at -20.
- Miniprepped overnight cultures of PL14-PL20 (~1:00 pm, STC)
- Using C1015 rotor, 6666 x g, the Corning culture tubes only fit in the centrifuge with the lids off
- Made LB, 3x 60 mL in 100 mL bottles (~ 3:00pm, SS)
- Made LB Agar, 4 x 250 mL LB Agar in 500 mL bottles (~3:00, CS)
- Autoclaved LB, LB Agar, and milliQ (~3:30 pm, SS)
- Made LB plates with Kan (~6:30 pm, CMR)
- CUGEM movie outing at 8:00 pm.
- Phusion PCR at 10:00 pm (DPW)
- Dylan's magic triple anneal method (57/65/70, 35 cycles total)
- Amplifying nah operon from Gibson 1
- Appending BioBrick cutsites for ligation into pSB3C5
June 30th, Saturday
- Took PCR out of thermal cycler at 9:00 am (DPW)
- Set up gel using NEB 100bp and 2-log ladders (10:00am)
- Continued gel extraction of p21 PCR digest from previous day (SS)
- Set up ligation of p21 PCR digest extraction and dephosphorylated pBBRBB+mtrB (11:11am, SS)
- Desalted ligation using Millipore membrane paper
- Transformed 2 electrocompetent DH5alpha stocks at 5:30 pm and 5:50 pm, respectively.
- Observed time constants for electroporation of 4.38 ms and 4.24 ms, respectively
- Let cells recover for 1 hour, plated on LB + Kan.
- Set up two ligations of pSB3C5 into [PNNL] electrocompetent Shewanella strain JG700 (6:30 pm, Sp.C and St.C)
- First transformation performed at usual PNNL voltage of 0.75 kV (time constant of 9.30 ms)
- Second transformation performed at [Myers and Myers] specification of 0.55 kV.
