Team:UNIPV-Pavia/Protocols/Transformation

From 2008.igem.org

Revision as of 23:14, 9 June 2008 by Lor18 (Talk | contribs)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Home.jpg Home Unipv logo.jpg The Team And.jpg The Project Safety.jpg Biological Safety Dna.png Parts Submitted to the Registry
Laptop.jpg Dry Lab Pipette.jpg Wet Lab Math.gif Modeling Note.jpg Protocols Notebook.gif Activity Notebook


Transformation

(estimated time: 3 hours and 30 min + 12-14 hours overnight incubation)

Materials needed:

  • LB agar plates with proper antibiotic added incubated at 37°C
  • Thawed Invitrogen TOP10 cells (every tube contains approximately 60 )
  • Resuspended DNA
  • SOC medium


  • Cut paper spots using scalpel and tweezers (or punch tool, following provided instructions); if you use scalpel and tweezers, try to cut pieces of about the same dimension of the punch tool.
  • Clean scalpel and tweezers (or punch tool) with water and ethanol every time you cut a spot; be careful to dry your tools correctly, especially if you use punch tool, which needs more time to dry than scalpel/tweezers.
  • Put the cut paper into the 0.5 ml tube.
  • Incubate at 42°C for 20 min.
  • Vortex and spin down.