Melbourne/Ligation Protocol

From 2007.igem.org

< Melbourne
Revision as of 11:33, 28 September 2007 by Craig (Talk | contribs)

<Return to list of protocols> <Team home page>

  • Applications: Ligate DNA fragments together


  • Time to complete protocol: Overnight, 2 hours, or 10 minutes
    • Lab time: 5 minutes
    • Waiting time: Overnight, 2h, 10min
  • Approximate cost of materials: $

Contents

Method from primary and secondary reagents

Primary & secondary Reagents Required including controls
Method including controls

Add to a sterile 1.7ml Eppendorf

  • Roughly an equal quantity of DNA fragments to be ligated together (usually 5ul of both vector and insert if gel-purified)
  • 2ul of 10X buffer or 10ul of 2X buffer
  • 1ul of T4 DNA ligase
  • milliQ water to make up to 20ul

Incubate Overnight (if using 10X buffer) at 4 degrees, 2h or 5min (if using 2X buffer) at room temprature.

Equipement Required
  • 1.5mL Microfuge tubes
  • Pipettes
  • Fridge
References