Difference between revisions of "Eckdahl-replication-protocol"
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- 7.6 uL water | - 7.6 uL water | ||
| − | - 10 uL 2x GoTaq | + | - 10 uL 2x GoTaq Green |
<b>New Chaperone PCR Thermal Profile</b> | <b>New Chaperone PCR Thermal Profile</b> | ||
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- Final extension: 74 degrees, 5 minutes | - Final extension: 74 degrees, 5 minutes | ||
| − | |||
| − | |||
<b>Origin PCR Mixture</b> | <b>Origin PCR Mixture</b> | ||
Revision as of 16:27, 4 June 2014
Procedures
Grow up E. coli from stock overnight
- One batch in amp, one in amp+chlor
- 4 mM caffeine
Prepare stock of .25 g/mL L-arabinose
- Add 2 mL of this stock to every L of LB+agar, for a final concentration of .5 mG/mL
Measure A590 (cell density) using Synergy/Cytation, dilute concentration to 0.1 with same LB+antibiotic+caffeine. Note that antibiotic will be amp for the 4 clones w/o chaperone, amp+chlor for 20 clones with chaperone.
Combine 0.5 mL of each clone.
Spread 50 uL with 15-20 beads onto Tet-only LB plates
- Prepare tetracycline-LB according to MWSU bacterial media protocol.
- Prepare caffeine disks (establish a precise method of preparing and placing disks, to minimize variation)
- Commercial disks (need to have a certain thickness to absorb enough solution)
- 35 uL 40 mM caffeine solution per disk
- Put dry disk on sterile petri dish, add caffeine (filter sterilized) and let sit for 1 minute
- Stab with the smallest sterile needle you have and transfer it to the tet plate, take sterile pipet tip and remove it from the needle.
- Let sit for 5 minutes with lid cracked open under sterile hood
- Incubate upside down
- 37degrees C overnight
- Room temperature for 4 days (with daily evaluation and regular photos and UV box photos)
Pick out each colony with sterile pipet tip and deposit in sterile microtiter plate/pcr tubes (LB+amp colony) filled with 10uL LB+amp. Mix well by pipetting up and down, using the same pipet tip for each colony. Number colonies and record whether each colony is big or little.
Pipet 5 uL of each LB+amp+clone to 195 LB+amp+chlor, using the same pipet tip for the same colony.
Add LB+amp to LB+amp clones to produce 200 uL LB+amp+clones, for each colony.
Incubate and measure A590 to determine how many colonies are still growing.
Measure RFP and GFP fluorescence
Spot each colony on a single plate (2 uL per spot)
Determine chaperone # with PCR; run on agarose gel
New Chaperone PCR Mixture
- 2 uL overnight culture of bacterial clone (picked out of amp+chlor)
- 0.4 uL primer cocktail with origin primers equally mixed from 100 uM stocks
- 7.6 uL water
- 10 uL 2x GoTaq Green
New Chaperone PCR Thermal Profile
- Initial denaturation: 10 minutes at 94 degrees
- 20 cycles of 94 degrees, 15 sec; 51 degrees, 15 sec; 74 degrees, 2 minutes
- Final extension: 74 degrees, 5 minutes
Origin PCR Mixture
- 2 uL overnight culture of bacterial clone (picked out of either amp or amp+chlor, according to the presence of the chaperone),
- 0.5 uL primer cocktail with origin primers equally mixed from 100 uM stocks
- 7.5 uL water
- 10 uL 2x GoTaq Green
Origin PCR Thermal Profile
- Initial denaturation: 94 degrees, 10 minutes
- 20 cycles of touch-down PCR: 94 degrees for 15 sec, 64.5 to 44.5 degrees for 15 sec; 74 degrees for 1 minute
- 20 cycles of PCR: 94 degrees for 15 sec, 44.5 degrees for 15 sec; 74 degrees for 1 minute
- Final extension: 74 degrees for 5 minutes
Plamids
J119346
– High promoter
– High C-dog (RBS)
– RFP
J119347
– Low promoter
– Low C-dog
– GFP
Origins
pSB1A2 High copy number
J119310 Low copy number
