=====Protocol for the Second Experiment 3/28/2012-4/9/2012===== ====Protocol==== //Goal: Grow large amounts of the pET28+CDS7 plasmid, grow up large amounts of the chlorophenicol biobrick backbone, restriction digest both and ligate the two together.// \\ - Streak both plasmids on a plate. grow O/N (Day 1) - Inoculate a few minicultures with colonies. grow O/N (Day 2) - Miniprep the minicultures (Day 3) - Verify plasmid using gel electrophoresis (Day 3) - Digest plasmid with restriction enzymes (Day 4) - Gel purify restriction digests (Day 5) - Ligate the purified products (Day 5) - Transform bacteria with ligation mixture. grow o/n (Day 6) - Inoculate miniculture of any successful transformants. grow o/n (Day 7) - Make glycerol stock (Day 8) - Miniprep/gel electrophoresis to verify (Day 9) * //Courtesy Dionne// * //Note: o/n denotes overnight// Back to [[start:classes:principlesofdesign:igem:start|iGEM]]