Team:Newcastle/Restriction digests

From 2010.igem.org

Revision as of 09:08, 27 July 2010 by Yessa (Talk | contribs)

iGEM Homepage Newcastle University BacillaFilla Homepage Image Map


To cut DNA at specific base sequences using restriction enzymes

Materials

The following are required to make a 30 µl solution:

  • 1 µl of restriction enzymes in total
  • 3 µl of 10x buffer
  • remainder is DNA/water

Notes

  • No more than 10% of enzyme - solution contains glycerol which inhibits reaction
  • 10x buffer must be diluted to 1x i.e. 10% final volume

Methods

  1. Load desired quantities of solution into microfuge tube
  2. Incubate at 37°C for 3 hours.