Team:Freiburg/Notebook/13 July

From 2011.igem.org

(Difference between revisions)
 
(One intermediate revision not shown)
Line 1: Line 1:
{{:Team:Freiburg/Templates/header}}
{{:Team:Freiburg/Templates/header}}
 +
<html>
 +
<div id="notebook-page-header">
 +
<div id="notebook-back" width="100px" >
 +
<a href="https://2011.igem.org/Team:Freiburg/Notebook/12_July">Previous entry</a>
 +
</div>
 +
<div id="notebook-title">
 +
<a href="https://2011.igem.org/Team:Freiburg/Notebook"> 13 July </a>
 +
</div>
 +
<div id="notebook-next">
 +
<a href="https://2011.igem.org/Team:Freiburg/Notebook/14_July">Next entry</a>
 +
</div>
 +
</div>
 +
</html>
 +
==<span style="color:red;">red light receptor</span>==
==<span style="color:red;">red light receptor</span>==
Line 19: Line 33:
|DNA concentration
|DNA concentration
|260/280
|260/280
-
|260|230
+
|260/230
|-
|-
|cph8a
|cph8a
Line 51: Line 65:
|1.81
|1.81
|}
|}
-
 
===Testdigest===
===Testdigest===

Latest revision as of 00:55, 22 September 2011


This is the wiki page
of the Freiburger student
team competing for iGEM 2011.
Thank you for your interest!

Contents

red light receptor

Investigators: Julia

Waiting for sequencing results of parts BBa_I15008 and BBa_I15009. Julia did Minipreps of single colonies with PCR-ampilfied Chp8 in pSB1T3. She also did a test digest to see if the insert is in the vector.

Miniprep

Investigators: Jakob

Miniprep of cph8 from M30109 in pSB1T3 DNA concentration was measured with NanoDrop:

samples DNA concentration 260/280 260/230
cph8a 33.7 1.79 1.74
cph8b 41.2 1.79 1.39
cph8c 24.1 1.87 1.47
cph8d 30 1.74 1.84
cph8e 34 1.81 1.86
cph8f 30 1.83 1.81

Testdigest

Investigators: Julia

Testdigest of cph8

  • Enzyme 1: EcoRI
  • Enzyme 2: PstI



Transformation

Investigators: Julia

Transformation of BBa_I15010 (in the vector pSB2K3) in cells. Sophie plated out the cells.

Comments: No colonies grew on the plates.


PCR

Investigators: Julia

New PCR for red light receptor.

Primer:

  • P10
  • P11

DNA template:

  • M30109

Comments: There were no bands on the gel.

Precipitator

Miniprep

Investigators: Sophie, Sandra

Comments: Ligation, transformation and picking of the clones was done before the miniprep was performed.

Miniprep of the plastik-binding domain: There were always picked two colonies of the same plate (sample and sample*).

sample / sample* DNA concentration 280/230 260/230
M2a alpha / M2a* alpha 66.5 / 91.6 1.84 / 1.75 1.76 / 1.40
M2a beta / M2a* beta 83.8 / 13.8 1.80 / 1.72 1.52 / 0.97
M2a gamma / M2a* gamma 118.9 / 56.1 1.68 / 1.86 1.00 / 2.13
M2a delta / M2a* delta 101.5 / 66.0 1.74 / 1.85 1.26 / 2.16
M2a epsilon / M2a* epsilon 112.9 / 69.9 1.68 / 1.82 1.00 / 1.82
M2b alpha / M2a* alpha 79.7 / 74.9 1.87 / 1.83 2.20 / 2.14
M2b Beta/M2b* beta 122.3/74.4 1.71/1.84 1.04/2.18
M2b gamma / M2b* gamma 111.2 / 72.0 1.70 / 1.83 1.08 / 1.99
M2b epsilon / M2b* epsilon 88.5 / 90.09 1.72 / 1.79 1.19 / 1.78
M3 alpha / M3* alpha 136.3 / 93.9 1.71 / 1.78 1.10 / 1.74
M3 beta / M3* beta 54.7 / 79.2 1.91 / 1.83 2.03 / 2.13
M3 gamma / M3* gamma 130.6 / 141.7 1.66 / 1.80 0.87 / 1.88
M3 delta / M3* delta 79.6 / 82.9 1.76 / 1.85 1.27 / 2.19
M3 epsilon / M3* epsilon 84.1 / 122.5 1.79 / 1.69 1.45 / 1.03



Testdigest

Investigators: Sophie

The minipreps were digested and loaded onto a gel.

                       

Retrieved from "http://2011.igem.org/Team:Freiburg/Notebook/13_July"