Melbourne/Ligation Protocol

From 2007.igem.org

< Melbourne(Difference between revisions)
(Primary & secondary Reagents Required including controls)
(Equipement Required)
 
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Add to a sterile 1.7ml Eppendorf
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)
*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
+
*2ul of [[Melbourne/primary 10X Ligase buffer|T4 Ligase buffer 10X]] or 10ul of [[Melbourne/primary 2X Ligase buffer|T4 Ligase buffer 2X]]
-
*1ul of T4 DNA ligase
+
*1ul of [[Melbourne/primary Ligase|T4 Ligase]]
-
*milliQ water to make up to 20ul
+
*[[Melbourne/primary milliq|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.
Incubate Overnight (if using 10X buffer) at 4 degrees, 2h or 5min (if using 2X buffer) at room temprature.
=====Equipement Required=====
=====Equipement Required=====
-
*1.5mL Microfuge tubes
+
*[[Melbourne/1.7ml microcentrifuge|microcentrifuge: 1.7ml]]
*Pipettes
*Pipettes
*Fridge
*Fridge
 +
=====References=====
=====References=====
*
*

Latest revision as of 11:37, 28 September 2007

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  • 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

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

Equipement Required
References