Team:Groningen/Labwork/12 July 2013

From 2013.igem.org

(Difference between revisions)
 
(4 intermediate revisions not shown)
Line 1: Line 1:
-
'''Mirjam'''
+
<html>
-
<br/>Made a PCR with (1) no strep tag (2) strep F (3) strep R. The annealing temperature for (1) and (2) is 78 degrees Celsius. For (3) the annealing temperature is 80 degrees Celsius.  
+
<head>
 +
<meta http-equiv="X-UA-Compatible" content="IE=EDGE" charset="utf-8" />
 +
<link rel="stylesheet" href="https://2013.igem.org/Team:Groningen/CSS/DefaultPage?action=raw&ctype=text/css" type="text/css" />
 +
</head>
 +
<body>
 +
 
 +
 
 +
<div id="header">
 +
  <img src="https://static.igem.org/mediawiki/2013/8/83/Groningen_slider2.jpg" width=100% height="220" >
 +
</div>
 +
 
 +
<div class="colmask threecol">
 +
 
 +
<span class="navigation">
 +
    </html>{{:Team:Groningen/Templates/Navigationbar}}<html>
 +
</span>
 +
 
 +
<span class="widgets">
 +
    </html>{{:Team:Groningen/Templates/facebook}}<html>
 +
</span>
 +
 
 +
<div class="mainContent">
 +
   
 +
 
 +
 
 +
<h2>Mirjam</h2>
 +
<br/>Made a <a href="https://2013.igem.org/Team:Groningen/protocols/PCR"><FONT COLOR="black"><b>PCR</b></FONT></a> with (1) no strep tag (2) strep F (3) strep R. The annealing temperature for (1) and (2) is 78 degrees Celsius. For (3) the annealing temperature is 80 degrees Celsius.  
Gel purification of the strep F silk obtained yesterday.
Gel purification of the strep F silk obtained yesterday.
-
<br/> Run a 0.8% agarose gel for 30 min at 90V.
+
<br/> Run a 0.8% agarose <a href="https://2013.igem.org/Team:Groningen/protocols/GelElectrophoresis"><FONT COLOR="black"><b>gel</b></FONT></a> for 30 min at 90V.
-
Made a gel for the PCR products. Four out of six revealed bands at the expected height.  
+
Made a <a href="https://2013.igem.org/Team:Groningen/protocols/GelElectrophoresis"><FONT COLOR="black"><b>gel</b></FONT></a> for the PCR products. Four out of six revealed bands at the expected height.  
-
Made a new ligation between digested munchen backbone and the LacI promoter.
+
Made a new <a href="https://2013.igem.org/Team:Groningen/protocols/Ligation"><FONT COLOR="black"><b>ligation</b></FONT></a> between digested munchen backbone and the LacI promoter.
Check of the restriction and ligation of the signal sequences and the silk. No bands appeared on gel.
Check of the restriction and ligation of the signal sequences and the silk. No bands appeared on gel.
-
'''Chaline'''
+
<h2>Chaline</h2>
<br/>Gel purification of the silk PCR products.
<br/>Gel purification of the silk PCR products.
-
'''Chaline and Mirjam'''
+
<h2>Chaline and Mirjam</h2>
-
<br/>Run a gel with the ligation product and the purified silk fragments.
+
<br/>Run a <a href="https://2013.igem.org/Team:Groningen/protocols/GelElectrophoresis"><FONT COLOR="black"><b>gel</b></FONT></a> with the ligation product and the purified silk fragments.
 +
<br/>Silk is present for all three kinds, although in a low concentration.
-
'''Inne'''
+
<h2>Inne</h2>
<br> Made 3 bottles of 250 ml LB Agar (20g/L LB, 16g/L Agar)
<br> Made 3 bottles of 250 ml LB Agar (20g/L LB, 16g/L Agar)
<br> Autoclaved:
<br> Autoclaved:
Line 26: Line 53:
<br> 1 bottle of milliQ (1 L)
<br> 1 bottle of milliQ (1 L)
-
Ran a gel with silk ligation at 100V for 22 min
+
Ran a <a href="https://2013.igem.org/Team:Groningen/protocols/GelElectrophoresis"><FONT COLOR="black"><b>gel</b></FONT></a> with silk ligation at 100V for 22 min
-
"'Sander and Claudio '"
+
<h2>Sander and Claudio</h2>
<br/>made antibiotic stock.
<br/>made antibiotic stock.
<br/>  Ampicillin 50mg/ml MQ water
<br/>  Ampicillin 50mg/ml MQ water
Line 34: Line 61:
<br/> Kanamycin 10mg/ml MQ water
<br/> Kanamycin 10mg/ml MQ water
<br/> Spectinomycin 10mg/ml MQ water
<br/> Spectinomycin 10mg/ml MQ water
 +
<br/> All stocks are filter sterilized and all except Chloramphenicol are stored at 4 degrees. Chloramphenicol is stored at -20 degrees
 +
   
 +
   
 +
</div>
 +
 +
 +
</div>
 +
 +
<div id="footer">
 +
  <p>iGEM 2013 Groningen</p>
 +
</div>
 +
 +
</body>
 +
</html>

Latest revision as of 10:14, 30 July 2013

Mirjam


Made a PCR with (1) no strep tag (2) strep F (3) strep R. The annealing temperature for (1) and (2) is 78 degrees Celsius. For (3) the annealing temperature is 80 degrees Celsius. Gel purification of the strep F silk obtained yesterday.
Run a 0.8% agarose gel for 30 min at 90V. Made a gel for the PCR products. Four out of six revealed bands at the expected height. Made a new ligation between digested munchen backbone and the LacI promoter. Check of the restriction and ligation of the signal sequences and the silk. No bands appeared on gel.

Chaline


Gel purification of the silk PCR products.

Chaline and Mirjam


Run a gel with the ligation product and the purified silk fragments.
Silk is present for all three kinds, although in a low concentration.

Inne


Made 3 bottles of 250 ml LB Agar (20g/L LB, 16g/L Agar)
Autoclaved:
3 bottles of demiwater (80 ml)
3 bottles of tabwater (80 ml)
3 bottles of milliQ (80 ml)
3 bottles of LB Agar (250 ml)
1 bottle of milliQ (1 L) Ran a gel with silk ligation at 100V for 22 min

Sander and Claudio


made antibiotic stock.
Ampicillin 50mg/ml MQ water
Chloramphenicol 5mg/ml Ethanol 50%
Kanamycin 10mg/ml MQ water
Spectinomycin 10mg/ml MQ water
All stocks are filter sterilized and all except Chloramphenicol are stored at 4 degrees. Chloramphenicol is stored at -20 degrees

Retrieved from "http://2013.igem.org/Team:Groningen/Labwork/12_July_2013"