Team:Tuebingen/Notebook/Protocols/control-restriction

From 2013.igem.org

(Difference between revisions)
Line 13: Line 13:
Control Restriction Digest
Control Restriction Digest
</div>
</div>
-
 
-
 
-
{{:Team:Tuebingen/Template/Tuebingen}}
 
-
 
-
<html>
 
-
<head>
 
-
<style>
 
-
 
-
</style>
 
-
</head>
 
-
 
-
<body>
 
-
 
-
<div id="actualHeadingOne">
 
-
Preparative Restriction Digest
 
-
</div>
 
-
 
<div id="actualContent">  
<div id="actualContent">  

Revision as of 02:01, 4 October 2013

Return to iGEM Main Page.

Control Restriction Digest
Back to Protocols

 

Reagents

1.5 µL 10x NEBuffer 2
0.15 µL 100x BSA
3 µL DNA from Mini-Prep (c > 50 ng/µL)
0.15 µL EcoRI or XbaI
0.15 µL PstI or SpeI
to 15 µL Aqua dest.

 

Procedure

  1. Around noon, mix all reagents in an 1.5 mL Eppendorf-tube and incubate at 37 °C until afternoon.
  2. Heat inactivate restriction enzymes at 80°C for 20 min.
  3. Add 1/10 volume of 10X Antarctic Phosphatase and mix. Incubate at 37 °C for 15 min for 5' extensions.
  4. Heat inactivate phosphatase at 70 °C for 5 min.
  5. Run control-gel in order to check a ligation / transformation.



</body>

</html>