Team:XMU-China/wetlabjournal

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AAA
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        <dd class="on">ABSTRACT</dd>
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        <dd class="out">PROGRESS</dd>
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<div class="tabcon">AAAAA</div>
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    <div class="tabcon dis"><span id="progresscss">Sunday, August 26th<br>
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Digital Display:
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Ligated 18AI and RETPcPb and put the ligation product in 16ºC overnight for the transformation in the next day.<hr>
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Time Delay:
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Goal: To do the ligation of pBAD-RBS0.6 and pBAD-RBS0.07.
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Isolate plasmids and ran on a gel. The result for analysis was correct. Cause the bands of pBAD hardly to be seem, we increased the volume of pBAD when ligation. <hr>
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Fluorescence Test:
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We changed the abrabinose concentration from high levels to lower ones according to last fluorescence measurements of PBADRLT. Besides, we took some kinetic curves in all concentration levels we had taken before for comparison. The analysis of these data will help us improve our efficiency in the coming fluorescence measurements<hr>
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Design:
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We did some card design and drew some drafts.<a href="https://2012.igem.org/Template:Team:XMU-China/wetlabjournal">[see more]</a></span>
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        DEVICE DESCRIPTION</p>
 
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      <p style=" font-size:28px; color:#004f7c">E.LUMOLI DISPLAYER</p>
 
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" width="133" height="141" style="float:right; "/>how to use balabala how 
 
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        use balabala how to use
 
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        balabala how to how to
 
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        use balabala how to use
 
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    balabala how to use balabala how to use how to use balabala how to use how to use balabala </p></div>
 
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      <td >Digital Display</td>
 
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      <td >Immobilization</td>
 
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      <td >&nbsp;</td>
 
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      <td width="300" bgcolor="#f8daef">Synthetic circuits with genetic logic gates, which compute extracellular and intracellular signals and elicit response differently. </td>
 
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      Immobilization of Fluorescent E.coli cells .Design A Bioreactor for Numeric Display  </td>
 
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Revision as of 16:27, 9 September 2012

XMU

XMU-Wet lab journal
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Retrieved from "http://2012.igem.org/Team:XMU-China/wetlabjournal"