Protocol/1
From 2010.igem.org
(Difference between revisions)
Line 39: | Line 39: | ||
{{Team:Alberta/endMainContent}} | {{Team:Alberta/endMainContent}} | ||
- | [[Team:Alberta/Protocols]] | + | [[Team:Alberta/Notebook/Protocols]] |
Revision as of 00:24, 26 October 2010
Protocol 1: Transformations
What you will need:
- Competent DH5α cells (50 uL per transformation)
- 2 uL of plasmid you want to transform
- 800 uL of LB (non-contaminated) per transformation
- Plate with correct antibiotics
Procedure:
- Chill a box of pipette tips at -4 C and put your reaction tubes on ice.
- Obtain DH5α cells from the –80 C freezer and thaw in palm. Just as they thaw, store on ice for 10 minutes.
- Use a chilled tip to transfer 50 ul of the DH5α cells into each tube. Set aside one tube as a control.
- Pipet 2uL of the plasmid (up to 25ng per 50 ul of competent cells, plasmid amt. should not exceed 5% that of the competent cells) into each tube. Swirl.
- Store on ice for 30 minutes.
- Place tubes in incubator set to 42 C for EXACTLY 90s.
- Return the tubes to ice for 2 min.
- Add 800uL of LB to each tube.
- Incubate at 37 C for 45 min, ensure that the tube has at least 2ml capacity, to properly aerate the cells.
- Spread cells on plate with appropriate antibiotic: plate between 50- 300ul each. Let dry.
- Place plates inverted in incubator at 37 C for 12-16 hours.
Team:Alberta/Notebook/Protocols