User:Andriana/7 June 2012
From 2012.igem.org
Contents |
I. Continued transformation of BL21 cells
II. Continued and finished Transformation of DH5-α cells:
NOTE: Conduct all procedures aseptically, sterilizing the lips of all containers used
- Dilute 2 mL of DH5-α cell solution grown overnight in 200 mL sterile LB broth and allow to grow until OD = .5 to .55
- Transfer all cell-broth solution into 4 polypropylene tubes
- Keep the tubes on ice for 10 minutes
- Centrifuge at 2500xg for 10 min at 4C.
- Pour off supernatant and remove as much LB from the pellet as possible by briefly letting the polypropylene tubes stand upside-down on kimwipes. Sterilize the lips of the tubes afterwards with flame.
- Resuspend pellets in each of the tubes with about 10 mL of TB buffer and combine solutions into 2 tubes containing about equal volumes. NOTE: If pellets are not dissolving from the bottom of test tubes, try either using a flame sterilized (burn alcohol-wet utensil) inoculating loop or glass stirring rod or sterile pipette tip to dislodge the pellets, but be careful not to contaminate the polypropylene tubes by touching them.
- Centrifuge the 2 test tubes at 2500xg for 10min at 4C again, draining the supernatant as in step 5.
- Resuspend the pellets in each of the polypropylene tubes with 10 mL TB buffer, and combine the solutions into one test tube.
- Add 1.5 mL DMSO and mix
- Store cells on ice for about 10 min. while putting out the sterile eppindorf tubes (chill on ice)
- Flash freeze cells with liquid nitrogen and store at -80C.
- Test:
- For contamination by plating on ampicillin plates
- For competency with a transformation
III. Plated BL21 cells and DH5-α cells on ampicillin plates to test for contamination
IV. Made more LB broth and autoclaved stock solutions and glassware