Team:DTU-Denmark/Lab protocols

From 2010.igem.org

Revision as of 09:43, 18 October 2010 by JulietFrederiksen (Talk | contribs)

Wiki banner 967px.png

Welcome to the DTU iGEM wiki!

Ligations

Preparation:

  1. Calculate your ligase concentration by estimation of DNA concentration from your restriction gel.
  2. Which vector to use?

Material:

  1. prepare ligation mix with a total volume of 20 μl
    • 2 μl 10x Buffer
    • Parts to be ligated: vector+insert 1:5, DNA conc. less than 50 ng
    • fill up with water
    • 1 μl ligase
    • control (no insert)
  2. Which vector to use?