Team:Groningen/Notebook/Wetwork 15August2012

From 2012.igem.org

(Difference between revisions)
 
Line 1: Line 1:
{{HeaderGroningen2012}}
{{HeaderGroningen2012}}
-
<div style="margin-left: 100px; margin-right:100px; color:white; font-size:12pt;">
+
<html>
 +
<head>
 +
<style type="text/css">
 +
p.margin
 +
{
 +
font-size:12pt;  
 +
line-height:14pt;  
 +
color:white;  
 +
 
 +
margin-top:0px;
 +
margin-bottom:20px;
 +
margin-left:150px;
 +
margin-right:250px;
 +
}
 +
 
 +
 
 +
</style>
 +
</head>
 +
<body><br><br><br>
 +
<p class="margin">
Tom <br>
Tom <br>
<br>
<br>
Line 19: Line 38:
Pigment used in this step: lycopene, amilCP, amilGFP <br>
Pigment used in this step: lycopene, amilCP, amilGFP <br>
Ligation was done for 2 hours in room temperature before continue to E. coli transformation. <br>
Ligation was done for 2 hours in room temperature before continue to E. coli transformation. <br>
-
 
+
<br>
-
<html>
+
<A HREF="https://2012.igem.org/Team:Groningen/Notebook"><FONT COLOR=#ff6700>Back to notebook</FONT></A>
<A HREF="https://2012.igem.org/Team:Groningen/Notebook"><FONT COLOR=#ff6700>Back to notebook</FONT></A>
 +
<br><br></p></body>
</html>
</html>
{{Template:SponsorsGroningen2012}}
{{Template:SponsorsGroningen2012}}

Latest revision as of 13:32, 26 September 2012







Tom

Ligation of alsT(150, 250, 300, 500) with GFP and psb1c3 and pfu promotor with GFP and psb1c3.
Result: Transformation in E.coli was succesfull.

PCR of GFP with preffix and suffix and PCR of GFP that can couple to pfu.
Result: only PCR product: GFP preffix suffix was succesfull.

Emeraldo
Sub-culturing the transformats colonies on LB agar plates

Nisa
Promoters-pigment cloning into pSB1C3. Molarity ratio plasmid:DNA insert = 1:3.
Promoter used in this step: fnr and lacI
Pigment used in this step: lycopene, amilCP, amilGFP
Ligation was done for 2 hours in room temperature before continue to E. coli transformation.

Back to notebook