Team:Lyon-INSA-ENS/Realisation/Protocols/Fermentas
From 2011.igem.org
(Difference between revisions)
(One intermediate revision not shown) | |||
Line 2: | Line 2: | ||
{{Lyon-INSA-ENS/blocStyle}} | {{Lyon-INSA-ENS/blocStyle}} | ||
{{INSA-Lyon/styletestaurelie}} | {{INSA-Lyon/styletestaurelie}} | ||
- | {{Lyon-INSA-ENS/ | + | {{Lyon-INSA-ENS/menuhorizontal}} |
- | {{Lyon-INSA-ENS/menuNotebookProtocoles}} | + | <!--{{Lyon-INSA-ENS/menuNotebookProtocoles}}--> |
+ | {{Lyon-INSA-ENS/menuNotebookVertical|Protocols = actif}} | ||
<html> | <html> |
Latest revision as of 10:19, 10 January 2012
Fermentas digestion
This protocol aims at cutting plasmids on specific restriction sites using restriction enzymes.
Procedure
1. In an eppendorf tube, add the following solutions in any order :
-250 ng DNA ( if the concentration is unknown, use 5µL )
-2.5µL (1X) or 5µL (2X) 10X tango buffer ( this depends on the enzymes used )
-water to get a volume of 25µL after addition of the enzymes
2. Add 1µL of each one of the desired enzymes.
3. Incubate at 37°C for 1h30
4. Incubate at 70°C for 10 mn to inactivate the restriction enzymes.