Team:TU Darmstadt/Protocols/Activity assay

From 2012.igem.org

(Difference between revisions)
 
(One intermediate revision not shown)
Line 27: Line 27:
    <li><a href="/Team:TU_Darmstadt/Safety" title="Safety">Safety</a></li>
    <li><a href="/Team:TU_Darmstadt/Safety" title="Safety">Safety</a></li>
    <li><a href="/Team:TU_Darmstadt/Downloads" title="Downloads">Downloads</a></li></ul></li>
    <li><a href="/Team:TU_Darmstadt/Downloads" title="Downloads">Downloads</a></li></ul></li>
-
<li><a href="/Team:TU_Darmstadt/Human_Practice" title="Human Practice">Human Practice</a><ul>
+
<li><a href="/Team:TU_Darmstadt/Human_Practice" title="Human Practice">Human Practice</a></li>   
-
    <li><a href="/Team:TU_Darmstadt/Human_Practice/Panel_Discussion " title="Panel Discussion">Panel Discussion</a></li>
+
-
    <li><a href="/Team:TU_Darmstadt/Human_Practice/Symposia" title="Symposia">Symposia</a></li>
+
-
    <li><a href="/Team:TU_Darmstadt/Human_Practice/Classes" title="Classes">Classes</a></li></ul></li>   
+
<li><a href="/Team:TU_Darmstadt/Sponsors" title="Sponsors">Sponsors</a><ul>
<li><a href="/Team:TU_Darmstadt/Sponsors" title="Sponsors">Sponsors</a><ul>
    <li><a href="/Team:TU_Darmstadt/Sponsors" title="Sponsors">Overview</a></li>
    <li><a href="/Team:TU_Darmstadt/Sponsors" title="Sponsors">Overview</a></li>
Line 45: Line 42:
* controll group is from the 6th point of same bacterial strain but carrying only [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808030 BBa_K808030] (RBS-PhoA-His6tag-pNBEst13-Myctag-EstA)  
* controll group is from the 6th point of same bacterial strain but carrying only [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808030 BBa_K808030] (RBS-PhoA-His6tag-pNBEst13-Myctag-EstA)  
* check every day for lysis area
* check every day for lysis area
-
=== LB-Agar-Bromthymol blue ===
+
=== LB-Agar-Bromothymol blue ===
* stick in six sterile PET particles  
* stick in six sterile PET particles  
* inoculate the PET particles with [https://2012.igem.org/Team:TU_Darmstadt/Materials/DH5alpha DH5&alpha;] containing pSB1C3-whole-construct and incubate at 37°C
* inoculate the PET particles with [https://2012.igem.org/Team:TU_Darmstadt/Materials/DH5alpha DH5&alpha;] containing pSB1C3-whole-construct and incubate at 37°C
* check every day for colour change (pH decrease when PET gets digested)
* check every day for colour change (pH decrease when PET gets digested)
* controll group is on LB-Agar-Bromthymol blue without arabinose
* controll group is on LB-Agar-Bromthymol blue without arabinose
 +
=== DYT-medium ===
=== DYT-medium ===
* inoculate 50 mL [https://2012.igem.org/Team:TU_Darmstadt/Materials/DYT DYT-medium]-CAM with bacteria containing [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808032 BBa_K808032]
* inoculate 50 mL [https://2012.igem.org/Team:TU_Darmstadt/Materials/DYT DYT-medium]-CAM with bacteria containing [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808032 BBa_K808032]

Latest revision as of 21:35, 26 September 2012

Contents

Activity Assays

ELISA Reader

LB-Agar-Tributyrin

  • inoculate the plate at 5 points with DH5α containing [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808032 BBa_K808032](L-arabinose regulated RBS-PhoA-His6tag-pNBEst13-Myctag-EstA) and incubate at 37°C
  • controll group is from the 6th point of same bacterial strain but carrying only [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808030 BBa_K808030] (RBS-PhoA-His6tag-pNBEst13-Myctag-EstA)
  • check every day for lysis area

LB-Agar-Bromothymol blue

  • stick in six sterile PET particles
  • inoculate the PET particles with DH5α containing pSB1C3-whole-construct and incubate at 37°C
  • check every day for colour change (pH decrease when PET gets digested)
  • controll group is on LB-Agar-Bromthymol blue without arabinose

DYT-medium

  • inoculate 50 mL DYT-medium-CAM with bacteria containing [http://partsregistry.org/wiki/index.php?title=Part:BBa_K808032 BBa_K808032]
  • incubate at 37°C to an OD600 = 0.6
  • incubate on ice for 15 min before inducing
  • prepare sterile test tubes
  • fill the tubes in the way shown in table 1
Component tst tube 1 test tube 2 test tube 3 test tube 4
DYT-medium x x x x
PET particle x x x
bacteria x x x
induced x x x
  • check every day the colour of the DYT-medium and take a picture
  • digestion of PET particles leads to a decreasing pH and will be shown by a yellow color