Team:Groningen/Notebook/Wetwork 12September2012

From 2012.igem.org

(Difference between revisions)
Line 15: Line 15:
margin-right:250px;
margin-right:250px;
}
}
 +
ul
 +
{
 +
font-size:12pt;
 +
line-height:14pt;
 +
color:white;
 +
margin-top:0px;
 +
margin-bottom:0px;
 +
margin-left:150px;
 +
margin-right:250px;
 +
 +
}
</style>
</style>
Line 37: Line 48:
</ul>
</ul>
<br>
<br>
-
12:30 SboA-GFP to micro-array test setup, start OD = 0.1 (see notebook Wetwork 02/09 and 27/06). Also put SboA-GFP and WT in normal 37 degrees stove (start OD = 0.1).<br>
+
<p class="margin">12:30 SboA-GFP to micro-array test setup, start OD = 0.1 (see notebook Wetwork 02/09 and 27/06). Also put SboA-GFP and WT in normal 37 degrees stove (start OD = 0.1).<br>
<br>
<br>
-
14:30 harvest cells<br>
+
<p class="margin">14:30 harvest cells<br>
<ul>
<ul>
<li>OD WT = 1.168</li>
<li>OD WT = 1.168</li>
Line 46: Line 57:
</ul>
</ul>
<br>
<br>
-
put cells on microscope slide for fluorescence microscopy:<br>
+
<p class="margin">put cells on microscope slide for fluorescence microscopy:<br>
<ul>agarose (1% in SMM) 500 uL on slide</li>
<ul>agarose (1% in SMM) 500 uL on slide</li>
<li>spread with glass plate</li>
<li>spread with glass plate</li>
Line 52: Line 63:
</ul>
</ul>
<br>
<br>
-
microscope results: no GFP, only autofluorescence.<br>
+
<p class="margin">microscope results: no GFP, only autofluorescence.<br>
<br><br>
<br><br>
Renske<br>
Renske<br>
<br>
<br>
-
put promoters of LMU Munchen in dh5a<br>
+
<p class="margin">put promoters of LMU Munchen in dh5a<br>
<br>
<br>
-
transformation of ~1 uL at 15:00<br>
+
<p class="margin">transformation of ~1 uL at 15:00<br>
-
mistake! forgot to add LB medium!! --> Plate out anyway (amp plates) + O/N 5 mL culture of the rest..<br>
+
<p class="margin">mistake! forgot to add LB medium!! --> Plate out anyway (amp plates) + O/N 5 mL culture of the rest..<br>
<br>
<br>
<br>
<br>
Line 67: Line 78:
<li>rfp-psac-cm in dh5a: 5x from 10/09 (new competent cells)</li>
<li>rfp-psac-cm in dh5a: 5x from 10/09 (new competent cells)</li>
</ul>
</ul>
-
at 15:00, 37 degrees C.<br>
+
<p class="margin">at 15:00, 37 degrees C.<br>
<br>
<br>

Revision as of 14:17, 26 September 2012







Tom/Renske/Elbrich

Test GFP: reaction to rotten meat

meat: 5 gram aliquot from freezer, 3 days at 20 degrees Celsius

tested:
Bacillus subtilis sp. 168 _ SboA_GFP in psac-cm (subjected to meat, and without meat) and WT (without meat)

11:00 inoculate O/N culture in SMM in normal 37 degrees stove.

  • OD SboA = 0.302
  • OD WT = 0.317

12:30 SboA-GFP to micro-array test setup, start OD = 0.1 (see notebook Wetwork 02/09 and 27/06). Also put SboA-GFP and WT in normal 37 degrees stove (start OD = 0.1).

14:30 harvest cells

  • OD WT = 1.168
  • OD SboA(no meat) = 1.023
  • OD SboA(meat) = 1.153

put cells on microscope slide for fluorescence microscopy:

    agarose (1% in SMM) 500 uL on slide
  • spread with glass plate
  • spot 1 uL of sample on slide (duplo)

microscope results: no GFP, only autofluorescence.


Renske

put promoters of LMU Munchen in dh5a

transformation of ~1 uL at 15:00

mistake! forgot to add LB medium!! --> Plate out anyway (amp plates) + O/N 5 mL culture of the rest..


O/N culture of:

  • rfp-psac-cm in dh5a: 2x from 9/09 (our competent cells)
  • rfp-psac-cm in dh5a: 5x from 10/09 (new competent cells)

at 15:00, 37 degrees C.

Back to notebook