Transformations

From 2008.igem.org

Transforming into DH5α or TOP10 E. coli

When transforming into DH5-alpha E.coli cells we followed the protocol below:

The plasmids we transformed were present in a 25µl ligation mixture (6µl of this being the vector plasmid, and 15µl of this being the digested plasmid in which the desired 2.2kb fragment was restricted out of).

  • On ice, add 12.5µl of the ligation mixture (see Ligating DNA protocol) to 100µl of DH5-alpha E.coli cells in an eppendorf tube
  • Mix well by pipetting up and down several times
  • Leave on ice for 45 minutes
  • Remove from ice and incubate for 3 minutes at 37˚C (this is the heat shock)
  • Add 300µl of LB and mix well with pipette
  • Incubate for 1 hour in a 37˚C water bath
  • Plate onto antibiotic agar (see Making Agar Plates )


Back to Team:Newcastle University/Protocols

Back to Team:Newcastle University/Notebook