Team:Macquarie Australia/Protocols/Ligation

From 2013.igem.org

(Difference between revisions)
 
(3 intermediate revisions not shown)
Line 4: Line 4:
<center>
<center>
<h1>Ligation Procedure</h1>
<h1>Ligation Procedure</h1>
-
</center>
 
-
 
<html lang="en">  
<html lang="en">  
<head>
<head>
Line 17: Line 15:
<div class="datagrid"><table>
<div class="datagrid"><table>
-
<!--     <table align="center"> Added by me -->
+
     <table align="center"> <!-- Added by me -->
<thead><tr><th>Element </th><th>Volume</th></tr></thead>
<thead><tr><th>Element </th><th>Volume</th></tr></thead>
<tbody><tr><td>Upstream Digestion part </td><td>2 µL</td></tr>
<tbody><tr><td>Upstream Digestion part </td><td>2 µL</td></tr>
Line 35: Line 33:
<br><br>
<br><br>
transform 4 µL of the ligation product into 100 µL of competent E. coli, then incubate the transformants for one hour.
transform 4 µL of the ligation product into 100 µL of competent E. coli, then incubate the transformants for one hour.
 +
 +
 +
[[File:LigationQLD.jpg|500px|thumb|center|Ligation]]

Latest revision as of 07:18, 13 September 2013


Ligation Procedure


Prepare the following reaction mixture

Element Volume
Upstream Digestion part 2 µL
Downstream Digestion part2 µL
Destination Plasmid1 µL
10X T4 DNA ligase buffer2 µL
T4 DNA ligase1 µL
H2O12 µL

Incubate each ligation mix at 30°C for 30 minutes, followed by heat inactivation at 80°C for 20 minutes.

transform 4 µL of the ligation product into 100 µL of competent E. coli, then incubate the transformants for one hour.


Ligation