Team:UNIK Copenhagen/Labbook

From 2014.igem.org

(Difference between revisions)
 
(5 intermediate revisions not shown)
Line 11: Line 11:
width: 900px;
width: 900px;
}
}
-
#all_content p, #all_content h1{
+
#all_content p{
-
font-family: "Courier New";
+
font-family: "Times New Roman", sans-serif;
 +
font-size:14px;
 +
}
 +
#all_content h1{
 +
font-family: "Lucinda sans unicode", sans-serif;
}
}
#all_content{
#all_content{
-
font-family: "Courier New";
 
margin: 30px;
margin: 30px;
padding: 0px;
padding: 0px;
Line 39: Line 42:
float: left;
float: left;
margin: 10px;
margin: 10px;
 +
}
 +
.content table{
 +
float: left;
 +
border: none;
 +
font-family: "Courier New";
 +
background-color: #FBF8EF;
 +
font-size: 12px;
 +
}
 +
.content table td{
 +
padding:0px 8px;
}
}
.left_page, .right_page{
.left_page, .right_page{
float: left;
float: left;
-
width: 375px;
+
width: 368px;
height: 526px;
height: 526px;
-
margin: 10px;
+
margin: 13px;
}
}
#items{
#items{
Line 135: Line 148:
</style>
</style>
-
</div>
 
Line 157: Line 169:
<div id="content1" class="content">
<div id="content1" class="content">
<div class="left_page">
<div class="left_page">
-
<p>Labbook is under contruction</p>
+
<p><b>17<sup>th</sup> of July - amplification of pETDuet-1 (Q)</b><br>
 +
Transformation of Ecloni with pETDuet-1 vector and plated the bacteria. They were afterwards stored in the fridge.<br><br>
 +
<b>23<sup>rd</sup> of July (Q)</b><br>We made three liquid cultures each from a single colony on the plate.<br><br>
 +
<b>24<sup>th</sup> of July(Q)</b><br>Minipreps of the pETDuet-1 vector. The minipreps was nanodroped. The measurements were:<br></p>
 +
 
 +
<table><tr>
 +
  <td>Colony:</td>
 +
  <td>ng/µl</td>
 +
  <td>260/280</td>
 +
  <td>260/230</td>
 +
</tr>
 +
<tr>
 +
  <td>1</td>
 +
  <td>30.3</td>
 +
  <td>1.96</td>
 +
  <td>2.34</td>
 +
</tr>
 +
<tr>
 +
  <td>2</td>
 +
  <td>63.3</td>
 +
  <td>1.82</td>
 +
  <td>1.89</td>
 +
</tr>
 +
<tr>
 +
  <td>3</td>
 +
  <td>32.1</td>
 +
  <td>1.82</td>
 +
  <td>1.68</td>
 +
</tr></table>
 +
<br><br><br><br><br>
 +
<p>On basis of the measurements, we picked sample 2 for sequencing. The sequences confirmed by sequencing.<br><br>
 +
<b>20<sup>st</sup> of August (Q)</b><br>
 +
Ecloni was  transformed with pUC57 containing sequences for either Estradiol light chain (EL) or Estradiol heavy chain (EH). The same was done for Progesterone light chain (PL) and heavy chain (PH). We also ran a PCR on pUC57, EL, EH, PL and PH.</p>
 +
 
</div>
</div>
<div class="right_page">
<div class="right_page">
-
<p>Content1 (right).</p>
 
-
 
</div>
</div>
</div>
</div>
Line 268: Line 311:
</div>
</div>
</div>
</div>
-
</div>
 
-
</html>
 
-
 
-
<html>
 
<div id="footer" style="position:absolute;bottom:0;">
<div id="footer" style="position:absolute;bottom:0;">
<hr><br>
<hr><br>

Latest revision as of 19:55, 27 August 2014




17th of July - amplification of pETDuet-1 (Q)
Transformation of Ecloni with pETDuet-1 vector and plated the bacteria. They were afterwards stored in the fridge.

23rd of July (Q)
We made three liquid cultures each from a single colony on the plate.

24th of July(Q)
Minipreps of the pETDuet-1 vector. The minipreps was nanodroped. The measurements were:

Colony: ng/µl 260/280 260/230
1 30.3 1.96 2.34
2 63.3 1.82 1.89
3 32.1 1.82 1.68





On basis of the measurements, we picked sample 2 for sequencing. The sequences confirmed by sequencing.

20st of August (Q)
Ecloni was transformed with pUC57 containing sequences for either Estradiol light chain (EL) or Estradiol heavy chain (EH). The same was done for Progesterone light chain (PL) and heavy chain (PH). We also ran a PCR on pUC57, EL, EH, PL and PH.

Content2 (left)

Content2 (right)

Content3 (left)

Content3 (right)

Content4 (left)

Content4 (right)

Content5 (left)

Content5 (right)

Content6 (left)

Content6 (right)

Content7 (left)

Content7 (right)

Content8 (left)

Content8 (right)

Content9 (left)

Content9 (right)

Content10 (left)

Content10 (right)

Retrieved from "http://2014.igem.org/Team:UNIK_Copenhagen/Labbook"