Team:Wisconsin-Madison/platereader

From 2011.igem.org

(Difference between revisions)
 
(5 intermediate revisions not shown)
Line 157: Line 157:
<a href="https://2011.igem.org/Team:Wisconsin-Madison">Main</a>
<a href="https://2011.igem.org/Team:Wisconsin-Madison">Main</a>
<a href="https://2011.igem.org/Team:Wisconsin-Madison/whatisigem">What is iGEM?</a>
<a href="https://2011.igem.org/Team:Wisconsin-Madison/whatisigem">What is iGEM?</a>
 +
<a href="https://2011.igem.org/Team:Wisconsin-Madison/ca">Contributions & Attributions</a>
</div>
</div>
</li>
</li>
Line 166: Line 167:
                 <a href="https://2011.igem.org/Team:Wisconsin-Madison/directedevolution">Directed Evolution</a>
                 <a href="https://2011.igem.org/Team:Wisconsin-Madison/directedevolution">Directed Evolution</a>
<a href="https://2011.igem.org/Team:Wisconsin-Madison/bmc">Microcompartment</a>
<a href="https://2011.igem.org/Team:Wisconsin-Madison/bmc">Microcompartment</a>
 +
                <a href="https://2011.igem.org/Team:Wisconsin-Madison/parts">Parts</a>
</div>
</div>
</li>
</li>
Line 179: Line 181:
<div id="m4" onmouseover="mcancelclosetime()" onmouseout="mclosetime()">
<div id="m4" onmouseover="mcancelclosetime()" onmouseout="mclosetime()">
<a href="https://2011.igem.org/Team:Wisconsin-Madison/protocols">Protocols</a>
<a href="https://2011.igem.org/Team:Wisconsin-Madison/protocols">Protocols</a>
-
<a href="https://2011.igem.org/Team:Wisconsin-Madison/calender">Calender</a>
+
<a href="https://2011.igem.org/Team:Wisconsin-Madison/calender">Calendar</a>
<a href="https://2011.igem.org/Team:Wisconsin-Madison/references">References</a>
<a href="https://2011.igem.org/Team:Wisconsin-Madison/references">References</a>
</div>
</div>
Line 188: Line 190:
<a href="https://2011.igem.org/Team:Wisconsin-Madison/reuposterSession">REU Poster Session</a>
<a href="https://2011.igem.org/Team:Wisconsin-Madison/reuposterSession">REU Poster Session</a>
<a href="https://2011.igem.org/Team:Wisconsin-Madison/socialmedia">Social Media</a>
<a href="https://2011.igem.org/Team:Wisconsin-Madison/socialmedia">Social Media</a>
-
<a href="https://2011.igem.org/Team:Wisconsin-Madison/presentations">Presentations</a>
 
</div>
</div>
</li>
</li>
<li><a href="https://2011.igem.org/Team:Wisconsin-Madison/safety" onmouseover="mopen('m6')" onmouseout="mclosetime()">Safety</a>
<li><a href="https://2011.igem.org/Team:Wisconsin-Madison/safety" onmouseover="mopen('m6')" onmouseout="mclosetime()">Safety</a>
 +
<div id="m6" onmouseover="mcancelclosetime()" onmouseout="mclosetime()">
 +
<a href="https://2011.igem.org/Team:Wisconsin-Madison/humanpractice">Human Practice</a>
 +
</div>
</li>
</li>
</ul>
</ul>
</center>
</center>
-
 
+
<center>
<center>
Line 214: Line 218:
<table border="0" cellspacing="4" cellpadding="0"><tr><td>
<table border="0" cellspacing="4" cellpadding="0"><tr><td>
-
<img src="https://static.igem.org/mediawiki/2011/f/fe/Plat_reader.jpg" width = "360" align="right"/>
+
<img src="https://static.igem.org/mediawiki/2011/f/fe/Plat_reader.jpg" width = "400" align="right"/>
<strong><font size="3">
<strong><font size="3">
Plate Reader (Fluorescence Detection)
Plate Reader (Fluorescence Detection)
Line 223: Line 227:
<p><br>
<p><br>
Learn more about <a href="https://2011.igem.org/Team:Wisconsin-Madison/biosensor">biosensors</a>.
Learn more about <a href="https://2011.igem.org/Team:Wisconsin-Madison/biosensor">biosensors</a>.
 +
<p>
 +
<font size="1"><i>About the image: Typical plate reader setup to test the efficacy of our EtOH sensor. Each lane is a sample, which was run in triplicate. The outer ring is blank media to prevent evaporation of the center samples.</i></font>
 +

Latest revision as of 23:00, 28 September 2011









Project >> Overview, Ethanol Sensor, Alkane Sensor, Microcompartment

Plate Reader (Fluorescence Detection)

To measure the fluorescence of our biosensor, we are using a Tecan ® Infinite™ Microplate Reader on 96 well plates. The outer ring of the plate is filled with a blank solution, typically the growth media used for the sensor, to prevent evaporation of the other samples in the plate. Each plate reader experiment is run to keep the optical densities (ODs) of each well as similar as possible, however, the OD is corrected later in the analysis of the data. Each row on the plate is a different sample, and each was run in triplicate. Plate reader protocols may be found in the protocols section.


Learn more about biosensors.

About the image: Typical plate reader setup to test the efficacy of our EtOH sensor. Each lane is a sample, which was run in triplicate. The outer ring is blank media to prevent evaporation of the center samples.