Team:TU Darmstadt/Materials/T4 DNA Ligase

From 2012.igem.org

(Difference between revisions)
(Created page with "<html> <link rel="stylesheet" href="https://2012.igem.org/wiki/index.php?title=Team:TU_Darmstadt/css&action=raw&ctype=text/css" type="text/css" /> <div id="TUD"> <div id="...")
(Supplier)
Line 46: Line 46:
For ligating extended oligos in a PCR reaction it is necessary to have [https://2012.igem.org/Team:TU_Darmstadt/Materials#Phosphatases phosphorilated] 5'-ends. Oligos will only be ligated when they are assembled on a compementary strand. <sup>[2]</sup>
For ligating extended oligos in a PCR reaction it is necessary to have [https://2012.igem.org/Team:TU_Darmstadt/Materials#Phosphatases phosphorilated] 5'-ends. Oligos will only be ligated when they are assembled on a compementary strand. <sup>[2]</sup>
=== Supplier ===
=== Supplier ===
-
* NEB http://www.neb.com/nebecomm/products/productR3133.asp
+
* NEB http://www.neb.com/nebecomm/products/productM0202.asp
 +
 
=== References ===
=== References ===
[1] http://en.wikipedia.org/wiki/DNA_ligase
[1] http://en.wikipedia.org/wiki/DNA_ligase
[2] http://openwetware.org/wiki/Thermostable_DNA_ligase
[2] http://openwetware.org/wiki/Thermostable_DNA_ligase

Revision as of 19:26, 11 September 2012

Contents

T4 DNA Ligase

About

T4 DNA ligase is an enzyme that facilitates the joining of DNA stands by catalyzing phosphodiester bonds. It was isolated from [http://en.wikipedia.org/wiki/Enterobacteria_phage_T4 bacteriophage T4] and is used to generate recombinant DNA sequences.[1]

Working conditions

For ligating extended oligos in a PCR reaction it is necessary to have phosphorilated 5'-ends. Oligos will only be ligated when they are assembled on a compementary strand. [2]

Supplier

  • NEB http://www.neb.com/nebecomm/products/productM0202.asp

References

[1] http://en.wikipedia.org/wiki/DNA_ligase

[2] http://openwetware.org/wiki/Thermostable_DNA_ligase