Team:Groningen/protocols/Ligation
From 2013.igem.org
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- | <br>All the reagents are added following the order listed in the table above. | + | <br>All the reagents are added following the order listed in the table above. |
+ | <br>After finishing the reaction mixture, the content is mixed and incubated at room temperature (~22°C) for 20 min. | ||
<br>Reference: http://www.thermoscientificbio.com/uploadedFiles/Resources/fast-digestion-dna.pdf | <br>Reference: http://www.thermoscientificbio.com/uploadedFiles/Resources/fast-digestion-dna.pdf | ||
Revision as of 15:34, 27 July 2013
Ligation
Materials:
- MQ water
- 1.5ml tubes
- Ligation buffer
- Ligase
- Insert
- Vector
Reaction:
Component | 20µl | Final concentration |
---|---|---|
MilliQ water | up to 20µl | |
10 ligation buffer | 2µl | 1x |
Vector | xµl | 20-100ng |
Insert | xµl | 3:1 molar ratio over vector |
T4 DNA ligase 5U/µl | 2µl | 0.5U/µl |
All the reagents are added following the order listed in the table above.
After finishing the reaction mixture, the content is mixed and incubated at room temperature (~22°C) for 20 min.
Reference: http://www.thermoscientificbio.com/uploadedFiles/Resources/fast-digestion-dna.pdf