Difference between revisions of "Team:NYMU-Taipei/Notebook-Lab Book-fruit flies hemolymph"

 
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@media screen and (min-width: 1000px){
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.technology{ /*header of 2nd demo*/
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<body>
 
<body>
  
<div id="wrap">
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  <div class="prototypeprototypesp">
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        <div class="imageimage00">
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            <img src="https://static.igem.org/mediawiki/2016/1/17/%E5%88%86%E9%A0%81_labnote_%E5%8A%A0%E5%AD%97%E7%89%88_labnote.jpg" width="100%" height="100%" />
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<div class="satisfy">
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        </div>
<h1>Lab note</h1></div>
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<h1>Lab note</h1></div>
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<hr />
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</div></div><br />
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<div class="prototypeprototype">
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<div id="wrap">
 
<div class="fund">
 
<div class="fund">
 
<h2 style="margin-top:30px; margin-bottom:10px;">Overview</h2><hr>
 
<h2 style="margin-top:30px; margin-bottom:10px;">Overview</h2><hr>
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<h2 style="margin-top:30px; margin-bottom:10px;">Related experiment schedule & Lab note</h2><hr>
 
<h2 style="margin-top:30px; margin-bottom:10px;">Related experiment schedule & Lab note</h2><hr>
<br /><p style="font-size:16px;">Experiments</p>
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<br /><h4 style="margin-top:30px; margin-bottom:10px;">Experiments</h4>
 
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 <tr>
     <td style="width:600px;">Bactro</td>
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     <td style="width:600px;">Bactrocera dorsalis</td>
 
     <td style="width:150px;">2</td>
 
     <td style="width:150px;">2</td>
 
     <td style="width:150px;">9/29~10/5</td>
 
     <td style="width:150px;">9/29~10/5</td>
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 <tr>
 
 <tr>
     <td style="width:600px;">Bactro</td>
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     <td style="width:600px;">Bactrocera dorsalis</td>
 
     <td style="width:150px;">2</td>
 
     <td style="width:150px;">2</td>
 
     <td style="width:150px;">9/29~10/5</td>
 
     <td style="width:150px;">9/29~10/5</td>
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<br /><p style="font-size:16px;">Experiments</p>
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<br /><h4 style="margin-top:30px; margin-bottom:10px;"">Routine works</h4>
  
 
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<center><p style="font-size:24px; color: #666666 !important; text-shadow: 0px 0px 1px #000000 !important; margin-bottom:100px;">
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style="color: #666666 !important; text-shadow: 0px 0px 1px #000000 !important;  /*margin: 12px !important;*/  font-size: 18px !important;  text-decoration: none;">[Collapse all]</a>  |
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<a href="#" onclick="ddaccordion.expandall('technology'); return false"
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style="color: #666666 !important; text-shadow: 0px 0px 1px #000000 !important;  /*margin: 12px !important;*/  font-size: 18px !important;  text-decoration: none;">[Expand all]</a></p></center></div>
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<div class="technology">8/23</div>
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<div class="thelanguage">
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<li><p style="font-size: 16px;">Oriental fruit flies sent to lab and cultivated by large transparent box to avoid oriental fruit flies flying out.</p></li>
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<div class="imageimage">
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<div style="position:relative; width:100%;">
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<img src="https://static.igem.org/mediawiki/2016/2/2a/T--NYMU-Taipei--photo-OFF-related-14724253_120300000672924380_2135741640_o.jpg" width="100%" /></div>
 
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 0); return false">[Collapse]</a></p>
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</div>
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<div class="technology">8/24</div>
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<div class="thelanguage">
 +
<li><p style="font-size: 16px;">We used both of centrifuge tube and feeding box to feed oriental fruit flies for comparing and ensuring the status of oriental fruit flies that established the independent space for observing oriental fruit flies.</p></li>
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<div class="imageimage">
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<div style="position:relative; width:100%;">
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<img src="https://static.igem.org/mediawiki/2016/4/42/T--NYMU-Taipei--photo-OFF-related-%E6%8B%8D%E7%85%A7.jpg" width="100%" /></div>
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</div>
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<br />
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<div class="imageimage">
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<div style="position:relative; width:48%;">
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<img src="https://static.igem.org/mediawiki/2016/3/3d/T--NYMU-Taipei--photo-OFF-related-14658400_120300000674554374_884455077_n.jpg" width="100%" /></div>
 +
<div style="position:relative; width:48%;">
 +
<img src="https://static.igem.org/mediawiki/2016/7/7d/T--NYMU-Taipei--photo-OFF-related-14686491_120300000678083870_2056369023_n.jpg" width="100%" /></div>
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</div>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 1); return false">[Collapse]</a></p>
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</div>
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<div class="technology">8/25</div>
 +
<div class="thelanguage">
 +
<li><p style="font-size: 16px;">B. dorsalis started to break through the cocoon. We conducted to put B. dorsalis to centrifuge tubes, avoiding the feeding box cannot load all oriental fruit flies. We poured the special agar to centrifuge tubes, and put centrifuges into entrance to catch oriental fruit flies. Then we sealed the centrifuge tubes by cotton. </li></p>
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<div class="imageimage">
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<div style="position:relative; width:100%;">
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<img src="https://static.igem.org/mediawiki/2016/5/5c/T--NYMU-Taipei--photo-OFF-related-14697277_120300000677127274_438898518_o.jpg" width="100%" /></div>
 +
</div>
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<p style="font-size: 16px;">(The team members put agar into centrifuge tubes which would be their feed.)</p>
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<div class="imageimage">
 +
<div style="position:relative; width:48%;">
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<img src="https://static.igem.org/mediawiki/2016/e/ea/T--NYMU-Taipei--photo-OFF-related-14741005_120300000677094868_1093963562_n.jpg" width="100%" /></div>
 +
<div style="position:relative; width:48%;">
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<img src="https://static.igem.org/mediawiki/2016/4/40/T--NYMU-Taipei--photo-OFF-related-14696947_120300000676485877_378050777_n.jpg" width="100%" /></div>
 +
</div>
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 +
<p style="font-size: 16px;">(The left picture is that oriental fruit flies broke through cocoon; the right picture is the feeding box & centrifuge tubes where fed oriental fruit flies.)</p>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 2); return false">[Collapse]</a></p>
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</div>
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<div class="technology">8/30</div>
 +
<div class="thelanguage">
 +
<li><p style="font-size: 16px;">First time to Conducting Experiment 1</p></li>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 3); return false">[Collapse]</a></p>
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</div>
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<div class="technology">9/3</div>
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<div class="thelanguage">
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<li><p style="font-size: 16px;">Changing the centrifuge tubes where oriental fruit flies lived. (Avoid the environment being mess.) /p></li>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 4); return false">[Collapse]</a></p>
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</div>
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<div class="technology">9/5</div>
 +
<div class="thelanguage">
 +
<li><p style="font-size: 16px;">Changing the centrifuge tubes where oriental fruit flies lived.</p></li>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 5); return false">[Collapse]</a></p>
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</div>
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<div class="technology">9/6</div>
 +
<div class="thelanguage">
 +
<li><p style="font-size: 16px;">The oriental fruit flies in centrifuge tubes are dead quickly, so we conducted trouble shooting and sent the mail to professors who research oriental fruit flies.</p></li>
 +
<li><p style="font-size: 16px;">We took the trap to Beitou orchard to try to catch oriental fruit flies. </p></li>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 6); return false">[Collapse]</a></p>
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</div>
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<div class="technology">9/7</div>
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<div class="thelanguage">
 +
<li><p style="font-size: 16px;">Second time to Conducting Experiment 1.</p></li>
 +
<li><p style="font-size: 16px;">Conducting trouble shooting.</p></li>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 7); return false">[Collapse]</a></p>
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</div>
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<div class="technology">9/10</div>
 +
<div class="thelanguage">
 +
<li><p style="font-size: 16px;">Searching the store selling the silkworm for extracting hemolymph which is used to induce pMcl1.</p></li>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 8); return false">[Collapse]</a></p>
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</div>
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 +
<div class="technology">9/13</div>
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<div class="thelanguage">
 +
<li><p style="font-size: 16px;">Visiting two farmers working in the orchard to ask the information about oriental fruit flies in the nature environment, and installing the trap of catching oriental fruit flies.</p></li>
 +
 +
<p style="font-size: 16px;">(Left picture: the team member install the trap; Right picture: the farmer and our team member took a picture)</p>
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<div class="imageimage">
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<div style="position:relative; width:50%; margin-right:10%;">
 +
<img src="https://static.igem.org/mediawiki/2016/d/d5/T--NYMU-Taipei--photo-OFF-related-14740977_120300000687733839_596021223_n.jpg" width="100%" /></div>
 +
<div style="position:relative; width:90%; margin-top:10%;">
 +
<img src="https://static.igem.org/mediawiki/2016/7/74/T--NYMU-Taipei--photo-OFF-related-14741635_120300000673924526_1894584987_n.jpg" width="100%" /></div>
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</div>
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<li><p style="font-size: 16px;">Sent the mail to researchers to ask for making public the content of the mail.</p></li>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 9); return false">[Collapse]</a></p>
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</div>
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<div class="technology">9/15</div>
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<div class="thelanguage">
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<li><p style="font-size: 16px;">Communicating with Chang Ming ecological education sericulture, asking the information of buying silkworm.</p></li>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 10); return false">[Collapse]</a></p>
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</div>
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<div class="technology">9/16</div>
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<div class="thelanguage">
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<li><p style="font-size: 16px;">Picking up the oriental fruit fly larval from rotten guavas and feeding them.</p></li>
 +
<li><p style="font-size: 16px;">Left picture: the team members were picking up the oriental fruit fly larval from rotten guavas; Right picture: the larval have picked up and put into another box.  Expected becoming pupae after six days. </p></li>
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<div class="imageimage">
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<div style="position:relative; width:48%;">
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<img src="https://static.igem.org/mediawiki/2016/f/f9/T--NYMU-Taipei--photo-OFF-related-14699910_120300000674856561_1048345374_n.jpg" width="100%" /></div>
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<div style="position:relative; width:48%;">
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<img src="https://static.igem.org/mediawiki/2016/e/e4/T--NYMU-Taipei--photo-OFF-related-14627744_120300000676522237_1703903936_n.jpg" width="100%" /></div>
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</div>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 11); return false">[Collapse]</a></p>
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</div>
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<div class="technology">9/22</div>
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<div class="thelanguage">
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<li><p style="font-size: 16px;">For the situation that our fruit flies in the centrifuge tubes were dead quickly , so we visited Dr. Yu-Bing Huang in Taiwan Agricultural Research Institute, Applied Zoology Division, and asking the problems about the right way for feeding oriental fruit flies. We change our way of feeding oriental fruit flies. </p></li>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 12); return false">[Collapse]</a></p>
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</div>
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<div class="technology">9/23</div>
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<div class="thelanguage">
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<li><p style="font-size: 16px;">Producing new feeding box which is larger and ventilation, and design the experimental boxes for Experiment 2: Infecting B. dorsalis with non-designed M. anisopliae.</p></li>
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<div class="imageimage">
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<div style="position:relative; width:48%;">
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<img src="https://static.igem.org/mediawiki/2016/9/91/T--NYMU-Taipei--photo-OFF-related-14697029_120300000683154255_1538186769_n.jpg" width="100%" /></div>
 +
<div style="position:relative; width:48%;">
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<img src="https://static.igem.org/mediawiki/2016/3/30/T--NYMU-Taipei--photo-OFF-related-14699699_120300000675475754_434414381_n.jpg" width="100%" /></div>
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</div>
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<p style="font-size: 16px;">(Left picture: experimental boxes; Right picture: the internal space of feeding box)</p>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 13); return false">[Collapse]</a></p>
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</div>
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<div class="technology">9/30</div>
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<div class="thelanguage">
 +
<li><p style="font-size: 16px;">The new oriental fruit flies broke through cocoon in the new feeding box</p></li>
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 +
<p style="font-size: 18px;">the new way for feeding oriental fruit flies is using gauze to be the windows that could be ventilation, and we can put watered agar and artificial feed on the top of gauze, then there were no water and feed in the box which lead to the environment being mess, and they also could have enough water and feed.</p>
 +
<br />
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<li><p style="font-size: 16px;">Infecting B. dorsalis with non-designed M. anisopliae started to conduct.</p></li>
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<div class="imageimage">
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<div style="position:relative; width:48%;">
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<img src="https://static.igem.org/mediawiki/2016/c/c5/T--NYMU-Taipei--photo-OFF-related-14696875_120300000677699020_204079543_n.jpg" width="100%" /></div>
 +
<div style="position:relative; width:48%;">
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<img src="https://static.igem.org/mediawiki/2016/4/46/T--NYMU-Taipei--photo-OFF-related-14696862_120300000674829370_219600743_n.jpg" width="100%" /></div>
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</div>
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<br />
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<div class="imageimage">
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<div style="position:relative; width:48%;">
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<img src="https://static.igem.org/mediawiki/2016/b/b9/T--NYMU-Taipei--photo-OFF-related-14686253_120300000675039507_1525612271_n.jpg" width="100%" /></div>
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<div style="position:relative; width:48%;">
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<img src="https://static.igem.org/mediawiki/2016/c/c7/T--NYMU-Taipei--photo-OFF-related-14627961_120300000679852339_2089167734_n.jpg" width="100%" /></div>
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</div>
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<p style="font-size: 16px;">Photos shows three concentration condition and negative control environment of experiment "Infecting B. dorsalis with non-designed M. anisopliae"</p>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 14); return false">[Collapse]</a></p>
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</div>
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<div class="technology">10/1</div>
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<div class="thelanguage">
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<li><p style="font-size: 16px;">Keeping on Experiment 2-1 (9/30~10/7)</p></li>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 15); return false">[Collapse]</a></p>
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</div>
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<div class="technology">10/7</div>
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<div class="thelanguage">
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<li><p style="font-size: 16px;">Experiment 2-1 finished.</p></li>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 16); return false">[Collapse]</a></p>
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</div>
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<div class="technology">10/10</div>
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<div class="thelanguage">
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<p style="font-size: 16px;">Experiment 2-2 "infecting female B. dorsalis by copulation with infected male B. dorsalis" started to conduct.</p>
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 17); return false">[Collapse]</a></p>
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</div>
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<div id="wrap">
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<div class="fund" style="white-space: pre-wrap;">
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<h2 style="margin-top:30px; margin-bottom:10px;">Q&A Section</h2><hr />
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<p style="font-size:16px;">How to CULTURE oriental fruit flies?</p>
 +
<p style="font-size:16px;"> The oriental fruit flies can grow in a transparent large container and centrifuge tubes with a piece of cotton placed at the opening to prevent them from escaping while still allowing air exchange.</p>
 +
<p style="font-size:16px;"> Feeding on sucrose-peptone agar (sited by ATCC) when you choose the centrifuge tubes as their living environment; a ratio of composition below is the way to feed the fruit flies in a larger container. The larval need the other formula to grow up whether living in the centrifuge tubes or the larger transparent container. The adult feeding formula without peptone can also alive the oriental fruit flies but not breeding.</p>
 +
<p style="font-size:16px;">                Larva formula                                            Adult formula ratio
 +
Yeast extraction 35g                      Sucrose: yeast extraction: peptone
 +
Sucrose 60g                      3:1:1
 +
Oat                 120g
 +
Sodium benzoate 1g
 +
Hydrochloric acid 4.5ml, 37%
 +
Water 450ml
 +
</p>
 +
<p style="font-size:16px;"> The advantage of cultivating in large container is avoiding the tight space that oriental fruit flies can almost only walk and then causing the growth medium spoil easily. On the other hand, cultivating the fruit flies in the centrifuge tubes can easily distinguish the situation of the oriental fruit flies, for example, gender, health, quantity to take the correct actions.</p>
 +
<p style="font-size:16px;">How to prevent COMTAMINATION?</p>
 +
<li><p style="font-size:16px;"></p>Adding preservatives, for instance, sodium benzoate, and decreasing environmental humidity can decease the growth of the mold on agar.</li>
 +
<li><p style="font-size:16px;"></p>Sterilize cotton according common lab procedure or just buy pre-sterilized one.</li><br />
 +
<p style="font-size:16px;">How do you KEEP the oriental fruit flies in place during experiments?</p>
 +
<li><p style="font-size:16px;"></p>Using carbon dioxide gas to induce comatose and try your best to contain the gas within the tube and the oriental fruit flies should be unconscious after 10-20 seconds.</li>
 +
<li><p style="font-size:16px;"></p>Induce coma under low temperature.</li><br />
 +
<p style="font-size:16px;">How about the methyl eugenol? Are there any suggestions on attracting the male oriental fruit flies or the actual situation that farmer using it to prevent the oriental fruit fly pest?</p>
 +
<li><p style="font-size:16px;">It is best to complete experiments using methyl eugenol before 2:00 PM.</p></li>
 +
<li><p style="font-size:16px;">Several time experiments may cause the male oriental fruit flies became desensitized to methyl eugenol, so it's important to change the sample you test on the experiments routinely to avoid the factor to interfere the result.</p></li>
 +
<li><p style="font-size:16px;">The attraction traps putting in the orchard need to add pure and undiluted methyl eugenol to capture the oriental fruit flies. It also needs some cottons or gauzes to separate the oriental fruit flies and methyl eugenol to prevent the chain of fruit flies and eventually causing the death.</p></li>
 +
<li><p style="font-size:16px;">It's not a good idea to set the trap when (a) it's a rainy day (b) it's not the harvest season of the guava or tangerine, or the number of the fruit flies captured will not high.</p></li><br />
 +
 +
 +
</div>
 +
 +
<div class="fund" style="white-space: pre;">
 +
 +
<h2 style="margin-top:30px; margin-bottom:10px;">Acknowledgements</h2><hr />
 +
 +
<p style="font-size:16px;">Beitou orchard
 +
S. J. Chen Grower
 +
</p>
 +
<p style="font-size:16px;">Beitou orchard
 +
Z. L. Liao Grower
 +
</p>
 +
<p style="font-size:16px;">Bioresource Collection and Research Center
 +
G. Y. Liou Fellow
 +
</p>
 +
<p style="font-size:16px;">Chiayi Agricultural Experiment Branch
 +
P. H. Chen Research assistant
 +
</p>
 +
<p style="font-size:16px;">Kaohsiung District Agricultural Research and Extension Station, COA, EY
 +
M. N. Tseng Research director
 +
</p>
 +
<p style="font-size:16px;">National Chung Hsing University, the Department of Entomology
 +
S. Y. Hwang Professor
 +
</p>
 +
<p style="font-size:16px;">National Chung Hsing University, the Department of Entomology
 +
Y. Y. Tseng Research assistant
 +
</p>
 +
<p style="font-size:16px;">Taiwan Agricultural Research Institute, Applied Zoology Division
 +
M. Y. Chiang Research assistant
 +
</p>
 +
<p style="font-size:16px;">Taiwan Agricultural Research Institute, Applied Zoology Division
 +
Y. B. Huang Professor
 +
/p>
 +
 +
</div>
 +
</div>
 +
 +
<script>if (window.runOnloadHook) runOnloadHook();</script></div>
 +
 +
<div class="prototypeprototypesp">
 +
<div id="wrap">
 +
<div class="fund">
 +
<h2 style="margin-top:10px; margin-bottom:10px;">Overview</h2><hr>
 +
 +
<p style="font-size:16px;">
 +
This section of our wiki contains the protocols for our insect experiments, including cultivation, infection rate tests, and hemolymph extraction.</p>
 +
 +
</div>
 +
 +
<div class="fund">
 +
 +
<h2 style="margin-top:30px; margin-bottom:10px; height:50px; line-height: 24px;">Related experiment schedule & Lab note</h2><hr>
 +
<h4 style="margin-top:30px; margin-bottom:10px;">Experiments</h4>
 +
 +
 +
<div class="tablesatisfysp" style="overflow-x:auto; margin-top:-50px;">
 +
<table border="1" >
 +
 <tr>
 +
     <td style="width:600px;">Experiments related to B. dorsalis</td>
 +
     <td style="width:150px;">Number</td>
 +
     <td style="width:150px;">Date</td>
 +
 </tr>
 +
 <tr>
 +
     <td style="width:600px;">Diameter of the tunnel that allows passage to one B. dorsalis</td>
 +
     <td style="width:150px;">1</td>
 +
     <td style="width:150px;">8/30~9/1</td>
 +
 </tr>
 +
 <tr>
 +
     <td style="width:600px;">Infecting B. dorsalis with non-designed M. anisopliae</td>
 +
     <td style="width:150px;">2-1</td>
 +
     <td style="width:150px;">9/30~10/7</td>
 +
 </tr>
 +
 <tr>
 +
     <td style="width:600px;">infecting female B. dorsalis by copulation with infected male B. dorsalis</td>
 +
     <td style="width:150px;">2-2</td>
 +
     <td style="width:150px;">10/10~10/17</td>
 +
 </tr>
 +
</table>
 +
</div>
 +
 +
<div class="tablesatisfysp" style="overflow-x:auto; margin-top:-50px;">
 +
<table border="1">
 +
 <tr>
 +
     <td style="width:600px;">Experiments about hemolymph extraction</td>
 +
     <td style="width:150px;">Number</td>
 +
     <td style="width:150px;">Date</td>
 +
 </tr>
 +
 <tr>
 +
     <td style="width:600px;">Blatta lateralis</td>
 +
     <td style="width:150px;">1</td>
 +
     <td style="width:150px;">9/20~9/30</td>
 +
 </tr>
 +
 <tr>
 +
     <td style="width:600px;">Bactrocera dorsalis</td>
 +
     <td style="width:150px;">2</td>
 +
     <td style="width:150px;">9/29~10/5</td>
 +
 </tr>
 +
 <tr>
 +
     <td style="width:600px;">Bombyx mori</td>
 +
     <td style="width:150px;">3</td>
 +
     <td style="width:150px;">10/3~10/</td>
 +
 </tr>
 +
</table>
 +
</div>
 +
<br /><h4 style="margin-top:30px; margin-bottom:10px;"">Routine works</h4>
 +
 +
<div class="tablesatisfysp" style="overflow-x:auto; margin-top:-50px;">
 +
<table border="1">
 +
 <tr>
 +
     <td style="width:750px;">Routine tasks of feeding Bactrocera dorsalis</td>
 +
     <td style="width:150px;">Date</td>
 +
 </tr>
 +
 <tr>
 +
     <td style="width:750px;">Produce & change the tube with the specific agar</td>
 +
     <td style="width:150px;">8/24~9/20</td>
 +
 </tr>
 +
 <tr>
 +
     <td style="width:750px;">Produce & change water gel and the specific ratio fodder</td>
 +
     <td style="width:150px;">9/22~10/</td>
 +
 </tr>
 +
</table>
 +
</div>
 +
 +
<div class="tablesatisfysp" style="overflow-x:auto; margin-top:-50px;">
 +
<table border="1">
 +
 <tr>
 +
     <td style="width:750px;">Routine tasks of hemolymph extraction</td>
 +
     <td style="width:150px;">Date</td>
 +
 </tr>
 +
 <tr>
 +
     <td style="width:750px;">Collect the mulberry leaves to feed the silkworm</td>
 +
     <td style="width:150px;">10/3~10/</td>
 +
 </tr>
 +
 <tr>
 +
     <td style="width:750px;">Sterilize the related equipments</td>
 +
     <td style="width:150px;">9/20~10/</td>
 +
 </tr>
 +
</table>
 +
</div>
 +
 +
</div>
 +
 +
</div><br /><br />
  
 
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style="color: #666666 !important; text-shadow: 0px 0px 1px #000000 !important;  /*margin: 12px !important;*/  font-size: 18px !important;  text-decoration: none;">[Expand all]</a></p></center></div>
 
style="color: #666666 !important; text-shadow: 0px 0px 1px #000000 !important;  /*margin: 12px !important;*/  font-size: 18px !important;  text-decoration: none;">[Expand all]</a></p></center></div>
  
<div class="technology">Week1</div>
+
<div class="technology">8/23</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">6/22: Received plasmid pFC330, pFC331, pFC332, pFC333 and pFC334 from Technical University of Denmark (Danish: Danmarks Tekniske Universitet)</p></li>
+
<li><p style="font-size: 16px;">Oriental fruit flies sent to lab and cultivated by large transparent box to avoid oriental fruit flies flying out.</p></li>
 +
 
 +
<div class="imageimage">
 +
<div style="position:relative; width:100%;">
 +
<img src="https://static.igem.org/mediawiki/2016/2/2a/T--NYMU-Taipei--photo-OFF-related-14724253_120300000672924380_2135741640_o.jpg" width="100%" /></div>
 +
</div>
  
 
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</div>
 
</div>
  
<div class="technology">Week2</div>
+
<div class="technology">8/24</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">6/29: Received plasmid pBARGPE1 From Bioresource Collection and Research Center</li></p>
+
<li><p style="font-size: 16px;">We used both of centrifuge tube and feeding box to feed oriental fruit flies for comparing and ensuring the status of oriental fruit flies that established the independent space for observing oriental fruit flies.</p></li>
<li><p style="font-size: 18px;">6/30: Received plasmids pCAMBIA1201 from Academia Sinica</li></p>
+
 
<li><p style="font-size: 18px;">6/30: Received plasmids pCAMBIA1300 from National Chung Hsing University</li></p>
+
<div class="imageimage">
<li><p style="font-size: 18px;">6/30: Received plasmid pTiB0542 from Academia Sinica</li></p>
+
<div style="position:relative; width:100%;">
 +
<img src="https://static.igem.org/mediawiki/2016/4/42/T--NYMU-Taipei--photo-OFF-related-%E6%8B%8D%E7%85%A7.jpg" width="100%" /></div>
 +
</div>
 +
<br />
 +
<div class="imageimage">
 +
<div style="position:relative; width:48%;">
 +
<img src="https://static.igem.org/mediawiki/2016/3/3d/T--NYMU-Taipei--photo-OFF-related-14658400_120300000674554374_884455077_n.jpg" width="100%" /></div>
 +
<div style="position:relative; width:48%;">
 +
<img src="https://static.igem.org/mediawiki/2016/7/7d/T--NYMU-Taipei--photo-OFF-related-14686491_120300000678083870_2056369023_n.jpg" width="100%" /></div>
 +
</div>
  
 
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<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 1); return false">[Collapse]</a></p>
 
</div>
 
</div>
  
<div class="technology">Week3</div>
+
<div class="technology">8/25</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">7/4: Received plasmid pVP-EL222 from University of Texas Southwestern</li></p>
+
<li><p style="font-size: 16px;">B. dorsalis started to break through the cocoon. We conducted to put B. dorsalis to centrifuge tubes, avoiding the feeding box cannot load all oriental fruit flies. We poured the special agar to centrifuge tubes, and put centrifuges into entrance to catch oriental fruit flies. Then we sealed the centrifuge tubes by cotton. </li></p>
<li><p style="font-size: 18px;">7/4: Received plasmid C120_empty from university of Texas Southwestern</li></p>
+
 
<li><p style="font-size: 18px;">7/4: Received plasmid ARSEF549 from ARSEF of USA</li></p>
+
<div class="imageimage">
<li><p style="font-size: 18px;">7/9: BBa_E1010 T-streaked onto agar plates</li></p>
+
<div style="position:relative; width:100%;">
 +
<img src="https://static.igem.org/mediawiki/2016/5/5c/T--NYMU-Taipei--photo-OFF-related-14697277_120300000677127274_438898518_o.jpg" width="100%" /></div>
 +
</div>
 +
 
 +
<p style="font-size: 16px;">(The team members put agar into centrifuge tubes which would be their feed.)</p>
 +
 
 +
<div class="imageimage">
 +
<div style="position:relative; width:48%;">
 +
<img src="https://static.igem.org/mediawiki/2016/e/ea/T--NYMU-Taipei--photo-OFF-related-14741005_120300000677094868_1093963562_n.jpg" width="100%" /></div>
 +
<div style="position:relative; width:48%;">
 +
<img src="https://static.igem.org/mediawiki/2016/4/40/T--NYMU-Taipei--photo-OFF-related-14696947_120300000676485877_378050777_n.jpg" width="100%" /></div>
 +
</div>
 +
 
 +
<p style="font-size: 16px;">(The left picture is that oriental fruit flies broke through cocoon; the right picture is the feeding box & centrifuge tubes where fed oriental fruit flies.)</p>
  
 
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</div>
 
</div>
  
<div class="technology">Week4</div>
+
<div class="technology">8/30</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">7/10: BBa_E1010 extracted the checked with restriction digestion (EocRI and PstI)</p></li>
+
<li><p style="font-size: 16px;">First time to Conducting Experiment 1</p></li>
<li><p style="font-size: 18px;">7/11: pBARGPE1 resuspended (from cryovial)</p></li>
+
<li><p style="font-size: 18px;">7/11: Transformed pBARGPE1 into competent cells</p></li>
+
<li><p style="font-size: 18px;">7/12: pBARGPE1 containing cultures used in 2 in 1</p></li>
+
<li><p style="font-size: 18px;">7/12: pBARGPE1 extracted from transformed cultures</p></li>
+
<li><p style="font-size: 18px;">7/13: pBARGPE1 checked with restriction digestion (EcoRI和SpeI)</p></li>
+
<li><p style="font-size: 18px;">7/13: pC120_empty resuspended (sample from University of Texas Southwestern)</p></li>
+
<li><p style="font-size: 18px;">7/13: pC120_empty transformation attempted (failed, no cultures on first plate)</p></li>
+
<li><p style="font-size: 18px;">7/13: pVP-EL222 resuspended (sample from University of Texas Southwestern)</p></li>
+
<li><p style="font-size: 18px;">7/13: pVP-EL222 transformed into competent cells</p></li>
+
<li><p style="font-size: 18px;">7/14: pVP-EL222 did 3 in 1</p></li>
+
<li><p style="font-size: 18px;">7/14: pVP-EL222 extracted from transformed cultures and checked with restriction digestion (EcoRI andXhoI)</p></li>
+
<li><p style="font-size: 18px;">7/14: pC120_empty transformation</p></li>
+
<li><p style="font-size: 18px;">7/15: pC120_empty extracted from transformed cultures and checked with PstI restriction digestion</p></li>
+
<li><p style="font-size: 18px;">7/15: pVP-EL222 plasmid stored and transformed cultures cryopreserved</p></li>
+
<li><p style="font-size: 18px;">7/16: pC120_empty plasmid stored and transformed cultures cryopreserved</p></li>
+
<li><p style="font-size: 18px;">7/16: BBa_E1010 checked with plasmid PCR (Primers: VF2-VR) (failed, no expected product)</p></li>
+
  
 
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</div>
 
</div>
  
<div class="technology">Week5</div>
+
<div class="technology">9/3</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">7/17: BBa_E1010 checked again with plasmid PCR (failed, probably due to primer VF2-FR malfunction)</p></li>
+
<li><p style="font-size: 16px;">Changing the centrifuge tubes where oriental fruit flies lived. (Avoid the environment being mess.) /p></li>
<li><p style="font-size: 18px;">7/18: BBa_E1010 checked with plasmid PCR with newly design primers</p></li>
+
<li><p style="font-size: 18px;">7/19: BBa_E1010 checked with plasmid PCR with the addition of Mg2+</p></li>
+
<li><p style="font-size: 18px;">7/21: pBARGPE1 plasmid stored and transformed cultures cryopreserved</p></li>
+
<li><p style="font-size: 18px;">7/22: Received plasmid pAN7-1 from Kaohsiung District Agricultural Research and Extension Station</p></li>
+
<li><p style="font-size: 18px;">7/22: Transformed plasmid pAN7-1 into competent cell</p></li>
+
<li><p style="font-size: 18px;">7/22: plasmid pAN7-1 did 2 in 1(liquid culture & second plate)</p></li>
+
<li><p style="font-size: 18px;">7/22: BBa_E1010 checked with Taq polymerase plasmid PCR (successful)</p></li>
+
<li><p style="font-size: 18px;">7/22: pAN7-1 transformation</p></li>
+
<li><p style="font-size: 18px;">7/22: pAN7-1 did 2 in 1</p></li>
+
<li><p style="font-size: 18px;">7/23: pAN7-1 plasmid extraction</p></li>
+
<li><p style="font-size: 18px;">7/23: Extracted plasmid pAN7-1</p></li>
+
<li><p style="font-size: 18px;">7/23: Transformed pCAMBIA1300 into competent cells</p></li>
+
  
 
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</div>
 
</div>
  
<div class="technology">Week6</div>
+
<div class="technology">9/5</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">7/24: pCAMBIA1300 containing cultures used in 2 in 1</p></li>
+
<li><p style="font-size: 16px;">Changing the centrifuge tubes where oriental fruit flies lived.</p></li>
<li><p style="font-size: 18px;">7/24: Extracted plasmid pCAMBIA1300</p></li>
+
<li><p style="font-size: 18px;">7/24: pCAMBIA1300 digestion check</p></li>
+
<li><p style="font-size: 18px;">7/24: pAN7-1 amplified with plasmid PCR (primer: minPgpdA)</p></li>
+
<li><p style="font-size: 18px;">7/24: pAN7-1 extracted and transformed cultures cryopreserved</p></li>
+
<li><p style="font-size: 18px;">7/24: pAN7-1 did plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">7/24: plasmid pAN7-1 stored plasmid and cryopreservation bacterical cultures</p></li>
+
<li><p style="font-size: 18px;">7/25: BBa_E1010 amplified with KOD polymerase PCR</p></li>
+
<li><p style="font-size: 18px;">7/26: pCAMBIA1300 stored plasmid and transformed cultures cryopreserved</p></li>
+
<li><p style="font-size: 18px;">7/26: RFP amplified with KOD polymerase PCR</p></li>
+
<li><p style="font-size: 18px;">7/26: RFP digested with EcoRI and BamHI</p></li>
+
<li><p style="font-size: 18px;">7/26: Amplified minimal PgpdA promoter on pAN7-1 by doing KOD PCR</p></li>
+
<li><p style="font-size: 18px;">7/26: pBARGPE1 digested for pBAR_RFP construction</p></li>
+
<li><p style="font-size: 18px;">7/27: PgpdA checked with Taq polymerase plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">7/28: Digested minimal PgpdA fragment for ligation with pC120_empty backbone to construct vector pC120_minPgpdA</p></li>
+
<li><p style="font-size: 18px;">7/28: pC120_empty ran restriction digestion for ligation with HindIII and BamHI (pC120_empty concentration was too low and contamination of the samples were detected)</p></li>
+
<li><p style="font-size: 18px;">7/29: VP-TR amplified with KOD polymerase PCR (failed, contaminated NC)</p></li>
+
<li><p style="font-size: 18px;">7/29: pVP-EL222 amplified with plasmid PCR (contaminated NC)</p></li>
+
<li><p style="font-size: 18px;">7/29: pBAR_RFP checked with KOD polymerase PCR (contaminated NC)</p></li>
+
<li><p style="font-size: 18px;">7/30: pVP-EL222 checked with plasmid PCR with brand new reagents (success, no contamination detected)</p></li>
+
<li><p style="font-size: 18px;">7/30: pC120_empty digestion for ligation with HindIII and BamHI</p></li>
+
<li><p style="font-size: 18px;">7/30: pBARGPE1 digested (concentration not high enough)</p></li>
+
  
 
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</div>
  
<div class="technology">Week7</div>
+
<div class="technology">9/6</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">7/31: Transformed C120_minimal PgpdA into competent cells</p></li>
+
<li><p style="font-size: 16px;">The oriental fruit flies in centrifuge tubes are dead quickly, so we conducted trouble shooting and sent the mail to professors who research oriental fruit flies.</p></li>
<li><p style="font-size: 18px;">7/31: C120_minimal PgpdA containing cells used in 2 in 1</p></li>
+
<li><p style="font-size: 16px;">We took the trap to Beitou orchard to try to catch oriental fruit flies. </p></li>
<li><p style="font-size: 18px;">7/31: pVP-EL222 amplified with plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">7/31: VP-TR trouble shooting</p></li>
+
<li><p style="font-size: 18px;">7/31: VP-TR PCR amplification</p></li>
+
<li><p style="font-size: 18px;">8/1: pVP-EL222 digested with SpeI and BamHI)</p></li>
+
<li><p style="font-size: 18px;">8/1: C120_minimal PgpdA extracted from transformed cells</p></li>
+
<li><p style="font-size: 18px;">8/1: pBARGPE1 digested for pBAR_RFP construction </p></li>
+
<li><p style="font-size: 18px;">8/1: RFP checked with PCR</p></li>
+
<li><p style="font-size: 18px;">8/1: C120_minimal PgpdA checked with restriction digestion</p></li>
+
<li><p style="font-size: 18px;">8/2: C120_minimal PgpdA amplified with plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">8/2: pBAR_RFP containing cultures used in 3 in 1</p></li>
+
<li><p style="font-size: 18px;">8/3: Extracted plasmid pBAR_RFP</p></li>
+
<li><p style="font-size: 18px;">8/3: pBAR_RFP did digestion check (wrong)</p></li>
+
<li><p style="font-size: 18px;">8/3: C120_minimal PgpdA digested for ligase with RFP</p></li>
+
<li><p style="font-size: 18px;">8/3: C120_minimal PgpdA_RFP transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">8/3: PgpdA checked with KOD polymerase plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">8/3: PgpdA amplified with KOD polymerase plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">8/3: RFP digested with EcoRI and BamHI for ligation </p></li>
+
<li><p style="font-size: 18px;">8/4: PgpdA digested for pBAR_PgpdA construction</p></li>
+
<li><p style="font-size: 18px;">8/4: C120_minimal PgpdA_RFP extracted from transformed cells</p></li>
+
<li><p style="font-size: 18px;">8/4: C120_minimal PgpdA_RFP amplified with plasmid PCR and checked with restriction digestion</p></li>
+
<li><p style="font-size: 18px;">8/4: pBARGPE1 digested for pBAR_EL222_TtrpC construction</p></li>
+
<li><p style="font-size: 18px;">8/5: pBARGPE1 digested for pBAR_PgpdA construction</p></li>
+
<li><p style="font-size: 18px;">8/5: pBAR_PgpdA transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">8/5: Transformed pBAR_RFP into competent cells</p></li>
+
<li><p style="font-size: 18px;">8/6: pBAR_RFP did 2 in1</p></li>
+
<li><p style="font-size: 18px;">8/6: pBAR_PgpdA containing cultures used in 2 in 1</p></li>
+
<li><p style="font-size: 18px;">8/6: C120_minimal PgpdA_RFP plasmid stored and transformed cultures cryopreserved</p></li>
+
  
 
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</div>
 
</div>
  
<div class="technology">Week8</div>
+
<div class="technology">9/7</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">8/7: pBAR_PgpdA extracted and checked with plasmid PCR and restriction digestion</p></li>
+
<li><p style="font-size: 16px;">Second time to Conducting Experiment 1.</p></li>
<li><p style="font-size: 18px;">8/8: Extracted plasmid pBAR_RFP</p></li>
+
<li><p style="font-size: 16px;">Conducting trouble shooting.</p></li>
<li><p style="font-size: 18px;">8/13: pBAR_RFP checked with restriction digestion</p></li>
+
<li><p style="font-size: 18px;">8/13: pBAR_RFP checked with plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">8/13: mRFP1 PCR amplification</p></li>
+
<li><p style="font-size: 18px;">8/13: TtrpC PCR amplification for VP- EL222_RFP</p></li>
+
  
 
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</div>
 
</div>
  
<div class="technology">Week9</div>
+
<div class="technology">9/10</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">8/14: pBAR_PgpdA plasmid stored and transformed cultures cryopreserved</p></li>
+
<li><p style="font-size: 16px;">Searching the store selling the silkworm for extracting hemolymph which is used to induce pMcl1.</p></li>
<li><p style="font-size: 18px;">8/14: C120_minimal PgpdA_RFP digested for ligation with TtrpC</p></li>
+
<li><p style="font-size: 18px;">8/15: C120_minimal PgpdA_RFP_TtrpC transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">8/15: pBARGPE1 digested for pBAR_mRFP1_TtrpC construction</p></li>
+
<li><p style="font-size: 18px;">8/15: pVP-EL222 amplified with PCR</p></li>
+
<li><p style="font-size: 18px;">8/15: TtrpC and pVP- EL222 PCR amplificaiton</p></li>
+
<li><p style="font-size: 18px;">8/16: TtrpC digestion</p></li>
+
<li><p style="font-size: 18px;">8/16: mRFP1 digestion</p></li>
+
<li><p style="font-size: 18px;">8/16: pBARGPE1 digested for pBAR_EL222_TtrpC construction</p></li>
+
<li><p style="font-size: 18px;">8/16: pBAR_EL222_TtrpC transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">8/16: pBAR_EL222_TtrpC containing cultures used 2 in 1</p></li>
+
<li><p style="font-size: 18px;">8/17: pBAR_EL222_TtrpC extracted and attempted to amplify with plasmid PCR------we did not amplify the target sequence (Hence, we tried ligation again)</p></li>
+
<li><p style="font-size: 18px;">8/17: C120_minimal PgpdA_RFP_TtrpC extracted and checked with restriction digestion</p></li>
+
<li><p style="font-size: 18px;">8/17: C120_minimal PgpdA_RFP_TtrpC amplified with plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">8/17: pBAR _RFP_TtrpC transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">8/17: pBAR _RFP_TtrpC containing cultures used in 2 in 1</p></li>
+
<li><p style="font-size: 18px;">8/18: pBAR _RFP_TtrpCdid extracted from transformed cultures and checked with restriction digestion</p></li>
+
<li><p style="font-size: 18px;">8/18: C120_minimal PgpdA_RFP_TtrpC plasmid stored and transformed bacterial cultures cryopreserved</p></li>
+
<li><p style="font-size: 18px;">8/18: pBAR_PgpdA digested for ligation with pVP-EL222 and TtrpC</p></li>
+
<li><p style="font-size: 18px;">8/18: pBAR_EL222_TtrpC transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">8/18: pBAR_EL222_TtrpC containing cultures used in 3 in 1</p></li>
+
<li><p style="font-size: 18px;">8/18: Amplified MCL1 promoter (PMCL1) from genome (Taq PCR from Metarhizium anisopliae ARSEF549 genomic DNA)</p></li>
+
<li><p style="font-size: 18px;">8/19: pBAR _RFP_TtrpC checked with restriction digestion------the incorrect bands appeared in gel electrophoresis results</p></li>
+
<li><p style="font-size: 18px;">8/19: mRFP1 PCR amplification (failed)</p></li>
+
<li><p style="font-size: 18px;">8/19: pBAR_EL222_TtrpC extracted from transformed cultures, checked with restriction enzyme digestion and plasmid PCR (failure)</p></li>
+
<li><p style="font-size: 18px;">8/19: pBAR_PgpdA_EL222_TtrpC transformed into competent cell </p></li>
+
<li><p style="font-size: 18px;">8/20: pVP-EL222 amplified with PCR than digested</p></li>
+
  
 
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</div>
 
</div>
  
<div class="technology">Week10</div>
+
<div class="technology">9/13</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">8/21: pBAR_PgpdA_EL222_TtrpC extracted and checked with restriction digestion (failure)</p></li>
+
<li><p style="font-size: 16px;">Visiting two farmers working in the orchard to ask the information about oriental fruit flies in the nature environment, and installing the trap of catching oriental fruit flies.</p></li>
<li><p style="font-size: 18px;">8/21: mRFP1 PCR amplification</p></li>
+
 
<li><p style="font-size: 18px;">8/21: mRFP1 digestion</p></li>
+
<p style="font-size: 16px;">(Left picture: the team member install the trap; Right picture: the farmer and our team member took a picture)</p>
<li><p style="font-size: 18px;">8/21: pBAR_PgpdA_EL222_TtrpC transformed into competent cell</p></li>
+
 
<li><p style="font-size: 18px;">8/22: PMCL1 Taq polymerase PCR amplification test run (failed, switched program afterwards)</p></li>
+
<div class="imageimage">
<li><p style="font-size: 18px;">8/23: PMCL1 KOD polymerase PCR amplification test run</p></li>
+
<div style="position:relative; width:50%; margin-right:10%;">
<li><p style="font-size: 18px;">8/23: PMCL1 Taq polymerase PCR amplification test run (with adjusted Mg2+ concentrations)</p></li>
+
<img src="https://static.igem.org/mediawiki/2016/d/d5/T--NYMU-Taipei--photo-OFF-related-14740977_120300000687733839_596021223_n.jpg" width="100%" /></div>
<li><p style="font-size: 18px;">8/23: TtrpC PCR amplification</p></li>
+
<div style="position:relative; width:90%; margin-top:10%;">
<li><p style="font-size: 18px;">8/23: TtrpC digestion</p></li>
+
<img src="https://static.igem.org/mediawiki/2016/7/74/T--NYMU-Taipei--photo-OFF-related-14741635_120300000673924526_1894584987_n.jpg" width="100%" /></div>
<li><p style="font-size: 18px;">8/23: pBAR_PgpdA_EL222_TtrpC containing cultures used in 3 in 1</p></li>
+
</div>
<li><p style="font-size: 18px;">8/23: BBa_E0040 containing cells T-streaked onto agar plates (failed to grow due to using incorrect antibiotics</p></li>
+
 
<li><p style="font-size: 18px;">8/24: pBAR_PgpdA_EL222_TtrpC checked with restriction digestion</p></li>
+
<li><p style="font-size: 16px;">Sent the mail to researchers to ask for making public the content of the mail.</p></li>
<li><p style="font-size: 18px;">8/24: pBAR_PgpdA_EL222_TtrpC amplified with plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">8/24: PMCL1 genome PCR amplification test run</p></li>
+
<li><p style="font-size: 18px;">8/24: NahR_GFP resuspended (from 2015 NYMU iGem team’s cryopreservation bacterical cultures)</p></li>
+
<li><p style="font-size: 18px;">8/24: NahR_GFP containing cultures used in 2 in 1</p></li>
+
<li><p style="font-size: 18px;">8/25: PMCL1 PCR amplification test run</p></li>
+
<li><p style="font-size: 18px;">8/25: pVP-EL222 checked separately with plasmid PCR with redesigned primers</p></li>
+
<li><p style="font-size: 18px;">8/25: mRFP1 checked with PCR due to multiple failed double ligation</p></li>
+
<li><p style="font-size: 18px;">8/26: mRFP1 checked with KOD polymerase PCR</p></li>
+
<li><p style="font-size: 18px;">8/26: mRFP1 amplified with KOD polymerase PCR</p></li>
+
<li><p style="font-size: 18px;">8/26: pVP-EL222 checked with plasmid PCR due to multiple failed ligations </p></li>
+
<li><p style="font-size: 18px;">8/26: pVP-EL222 checked with restriction digestion due to multiple failed ligations</p></li>
+
<li><p style="font-size: 18px;">8/26: pVP-EL222 checked with Taq polymerase plasmid PCR with remixed primers</p></li>
+
<li><p style="font-size: 18px;">8/26: PMCL1 KOD polymerase PCR amplification test run</p></li>
+
<li><p style="font-size: 18px;">8/26: TtrpC KOD PCR check(with remixed pVP- EL222 primers)</p></li>
+
<li><p style="font-size: 18px;">8/27: TtrpC KOD PCR amplification</p></li>
+
<li><p style="font-size: 18px;">8/27: BBa_E0040 containing cells T-streaked onto agar plates</p></li>
+
<li><p style="font-size: 18px;">8/27: mRFP1 and TtrpC PCR ligation</p></li>
+
<li><p style="font-size: 18px;">8/27: pBARGPE1 checked with restriction digestion due multiple failed attempts to ligate pBARGPE1 with various inserts</p></li>
+
<li><p style="font-size: 18px;">8/27: pVP-EL222 checked with KOD polymerase plasmid PCR with remixed primers</p></li>
+
<li><p style="font-size: 18px;">8/27: pVP-EL222 amplified with PCR (use for ligation with both pBAR_PgpdA and PMCL1)</p></li>
+
  
 
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</div>
  
<div class="technology">Week11</div>
+
<div class="technology">9/15</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">8/28: RFP_TtrpC digested for ligation with pBARGPE1------ the concentration was not high enough
+
<li><p style="font-size: 16px;">Communicating with Chang Ming ecological education sericulture, asking the information of buying silkworm.</p></li>
<li><p style="font-size: 18px;">8/28: RFP and TtrpC did PCR to ligase(failure, we change the volume of the primer and Mg2+)</p></li>
+
<li><p style="font-size: 18px;">8/28: EL222 and TtrpC ran ligation PCR ------- NC had band </p></li>
+
<li><p style="font-size: 18px;">8/28: EL222 and TtrpC ran ligation PCR ------ with remixed primer</p></li>
+
<li><p style="font-size: 18px;">8/28: pVP-EL222 and TtrpC PCR ligation ------- NC had bands </p></li>
+
<li><p style="font-size: 18px;">8/28: pVP-EL222 and TtrpC PCR ligation ------- used remixed primer</p></li>
+
<li><p style="font-size: 18px;">8/29: pVP-EL222 and TtrpC PCR ligation ------- the concentration was not high enough after gel extraction </p></li>
+
<li><p style="font-size: 18px;">8/29: EL222 and TtrpC ran ligation PCR ------ the concentration was not high enough after gel extraction </p></li>
+
<li><p style="font-size: 18px;">8/31: EL222 and TtrpC ran ligation PCR </p></li>
+
<li><p style="font-size: 18px;">8/31: pBAR_RFP digestion(to transformed into meta)</p></li>
+
<li><p style="font-size: 18px;">8/31: RFP_TtrpC digested for ligase with pBARGPE1 (the band existed on wrong site)</p></li>
+
<li><p style="font-size: 18px;">8/31: pVP-EL222 and TtrpC PCR ligation</p></li>
+
<li><p style="font-size: 18px;">8/31: PMCL1 Taq polymerase PCR amplification </p></li>
+
<li><p style="font-size: 18px;">9/1: PMCL1 PCR amplification test run</p></li>
+
<li><p style="font-size: 18px;">9/1: PMCL1 KOD polymerase PCR amplification</p></li>
+
<li><p style="font-size: 18px;">9/1: PMCL1 polymerase PCR amplification</p></li>
+
<li><p style="font-size: 18px;">9/1: RFP_TtrpC digested</p></li>
+
<li><p style="font-size: 18px;">9/1: pVP-EL222 and TtrpC PCR ligase </p></li>
+
<li><p style="font-size: 18px;">9/1: EL222 and TtrpC ran ligation PCR </p></li>
+
<li><p style="font-size: 18px;">9/2: EL222-TtrpC digestion</p></li>
+
<li><p style="font-size: 18px;">9/2: pBARGPE1 digested for pBAR_EL222_TtrpC construction</p></li>
+
<li><p style="font-size: 18px;">9/2: pBAR _RFP_TtrpC transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">9/2: pBAR_PgpdA digested for ligation with EL222_TtrpC</p></li>
+
<li><p style="font-size: 18px;">9/2: PMCL1 KOD polymerase PCR amplification</p></li>
+
<li><p style="font-size: 18px;">9/2: PMCL1 KOD polymerase PCR amplification</p></li>
+
<li><p style="font-size: 18px;">9/3: PMCL1 KOD polymerase PCR amplification</p></li>
+
<li><p style="font-size: 18px;">9/3: pBAR_EL222_TtrpC transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">9/3: pBAR_EL222_TtrpC containing cultures used in 3 in 1</p></li>
+
<li><p style="font-size: 18px;">9/3: pBAR_PgpdA digested for ligation with EL222_TtrpC</p></li>
+
<li><p style="font-size: 18px;">9/3: pBAR_PgpdA_EL222_TtrpC transformed into competent cell</p></li>
+
  
 
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</div>
  
<div class="technology">Week12</div>
+
<div class="technology">9/16</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">9/4: pBAR_PgpdA_EL222_TtrpC containing cultures used in 3 in 1</p></li>
+
<li><p style="font-size: 16px;">Picking up the oriental fruit fly larval from rotten guavas and feeding them.</p></li>
<li><p style="font-size: 18px;">9/4: pBAR_PgpdA_EL222_TtrpC extracted from transformed cultures</p></li>
+
<li><p style="font-size: 16px;">Left picture: the team members were picking up the oriental fruit fly larval from rotten guavas; Right picture: the larval have picked up and put into another box.  Expected becoming pupae after six days. </p></li>
<li><p style="font-size: 18px;">9/4: pBAR _RFP_TtrpC did plasmid PCR</p></li>
+
 
<li><p style="font-size: 18px;">9/4: PMCL1 KOD polymerase PCR amplification </p></li>
+
<div class="imageimage">
<li><p style="font-size: 18px;">9/5: pBAR _RFP_TtrpC transformed into competent cell ------ there was no E.coli on the first plate</p></li>
+
<div style="position:relative; width:48%;">
<li><p style="font-size: 18px;">9/5: mRFP1 amplified with KOD polymerase PCR</p></li>
+
<img src="https://static.igem.org/mediawiki/2016/f/f9/T--NYMU-Taipei--photo-OFF-related-14699910_120300000674856561_1048345374_n.jpg" width="100%" /></div>
<li><p style="font-size: 18px;">9/5: pBAR_PgpdA_EL222_TtrpC amplified with plasmid PCR</p></li>
+
<div style="position:relative; width:48%;">
<li><p style="font-size: 18px;">9/5: pBAR_EL222_TtrpC checked with restriction enzyme digestion</p></li>
+
<img src="https://static.igem.org/mediawiki/2016/e/e4/T--NYMU-Taipei--photo-OFF-related-14627744_120300000676522237_1703903936_n.jpg" width="100%" /></div>
<li><p style="font-size: 18px;">9/6: EL222-TtrpC digestion</p></li>
+
</div>
<li><p style="font-size: 18px;">9/6: pBAR_EL222_TtrpC checked with restriction enzyme digestion</p></li>
+
<li><p style="font-size: 18px;">9/6: pBAR_PgpdA_EL222_TtrpC checked with restriction digestion (failure)</p></li>
+
<li><p style="font-size: 18px;">9/6: pBAR_PgpdA_EL222_TtrpC checked with restriction digestion (we changed  enzymes)</p></li>
+
<li><p style="font-size: 18px;">9/6: EL222-TtrpC checked with restriction digestion</p></li>
+
<li><p style="font-size: 18px;">9/6: EL222-TtrpC digested with restriction enzyme</p></li>
+
<li><p style="font-size: 18px;">9/6: BBa_E0040 streaked onto agar plates</p></li>
+
<li><p style="font-size: 18px;">9/6: BBa_K118400 resuspended from 2016 iGEM Kit plate 4</p></li>
+
<li><p style="font-size: 18px;">9/6: BBa_K118400 transformed into competent cells</p></li>
+
<li><p style="font-size: 18px;">9/6: pBAR _RFP_TtrpC transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">9/6: PMCL1 KOD polymerase PCR amplification</p></li>
+
<li><p style="font-size: 18px;">9/6: PMCL1 KOD polymerase PCR amplification</p></li>
+
<li><p style="font-size: 18px;">9/7: PMCL1 KOD polymerase PCR amplification</p></li>
+
<li><p style="font-size: 18px;">9/7: pBAR _RFP_TtrpC transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">9/7: pBAR _RFP_TtrpC did 2 in 1</p></li>
+
<li><p style="font-size: 18px;">9/7: pBAR _RFP_TtrpC did 3 in 1</p></li>
+
<li><p style="font-size: 18px;">9/7: BBa_E0040 cultures used in 2 in 1</p></li>
+
<li><p style="font-size: 18px;">9/7: pBAR_EL222 PCR</p></li>
+
<li><p style="font-size: 18px;">9/7: BBa_K118400 containing culture used in 2 in 1</p></li>
+
<li><p style="font-size: 18px;">9/7: pVP-EL222 amplified with PCR (use for ligation with both pBAR_PgpdA and PMCL1)</p></li>
+
<li><p style="font-size: 18px;">9/8: pVP-EL222 amplified with PCR (use for ligation with both pBAR_PgpdA and PMCL1)</p></li>
+
<li><p style="font-size: 18px;">9/8: BBa_K118400 extraction extracted from transformed cultures</p></li>
+
<li><p style="font-size: 18px;">9/8: BBa_K118400 amplified with plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">9/8: BBa_E0040 extracted from transformed culture</p></li>
+
<li><p style="font-size: 18px;">9/8: pBAR _RFP_TtrpC plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">9/8: pBAR _RFP_TtrpC digestion check</p></li>
+
<li><p style="font-size: 18px;">9/8: pBAR _RFP_TtrpC digestion check</p></li>
+
<li><p style="font-size: 18px;">9/8: pBAR _RFP_TtrpC did plasmid extraction</p></li>
+
<li><p style="font-size: 18px;">9/8: PMCL1 KOD polymerase PCR amplification</p></li>
+
<li><p style="font-size: 18px;">9/9: PMCL1 KOD polymerase PCR amplification</p></li>
+
<li><p style="font-size: 18px;">9/9: pBAR _RFP_TtrpC did digestion check</p></li>
+
<li><p style="font-size: 18px;">9/9: BBa_E0040 amplified in plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">9/9: mRFP1amplified with KOD polymerase PCR</p></li>
+
<li><p style="font-size: 18px;">9/9: BBa_E0040 checked with restriction digestion (successful)</p></li>
+
<li><p style="font-size: 18px;">9/9: BBa_K118400 checked with restriction digestion (the gel had faulty matrix)</p></li>
+
<li><p style="font-size: 18px;">9/9: BBa_K118400 checked with restriction digestion (confirmed, successful)</p></li>
+
<li><p style="font-size: 18px;">9/9: BBa_K1184000 use KOD polymerase to amplify the target part KillerRed (try)</p></li>
+
<li><p style="font-size: 18px;">9/9: pBAR_PgpdA_EL222_TtrpC checked with restriction digestion</p></li>
+
<li><p style="font-size: 18px;">9/9: pBAR_PgpdA_EL222_TtrpC transformed into competent cell( there was no E.coli on our first plate )</p></li>
+
<li><p style="font-size: 18px;">9/9: pBARGPE1 digested for pBAR_mRFP1_TtrpC construction </p></li>
+
<li><p style="font-size: 18px;">9/10: pBARGPE1 digested for pBAR_PgpdA_EL222_TtrpC construction</p></li>
+
<li><p style="font-size: 18px;">9/10: pBAR_PgpdA_EL222_TtrpC transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">9/10: BBa_K1184000 use KOD polymerase to amplify the target part KillerRed (really amplified)</p></li>
+
<li><p style="font-size: 18px;">9/10: RFP and TtrpC use primer to ligase</p></li>
+
<li><p style="font-size: 18px;">9/10: RFP_TtrpC PCR to amplify the target sequence</p></li>
+
<li><p style="font-size: 18px;">9/10: Digested KillerRed fragment and its backbone pBARGPE1 with BamHI and EcoRI for ligation to construct the vector pBAR_KR</p></li>
+
<li><p style="font-size: 18px;">9/10: Digested KillerRed fragment and its backbone pBARGPE1 with BamHI and EcoRI again</p></li>
+
<li><p style="font-size: 18px;">9/10: Amplified PMCL1 from genome (KOD polymerase)</p></li>
+
<li><p style="font-size: 18px;">9/10: Amplified PMCL1 from genome (KOD polymerase)</p></li>
+
<li><p style="font-size: 18px;">9/10: Standard part PgpdA amplification PCR with Taq polymerase</p></li>
+
  
 
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<div class="technology">Week13</div>
+
<div class="technology">9/22</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">9/11: Standard part PgpdA amplification PCR with KOD polymerase</p></li>
+
<li><p style="font-size: 16px;">For the situation that our fruit flies in the centrifuge tubes were dead quickly , so we visited Dr. Yu-Bing Huang in Taiwan Agricultural Research Institute, Applied Zoology Division, and asking the problems about the right way for feeding oriental fruit flies. We change our way of feeding oriental fruit flies. </p></li>
<li><p style="font-size: 18px;">9/11: pBARGPE1 digested for pBAR_PgpdA_EL222_TtrpC construction</p></li>
+
<li><p style="font-size: 18px;">9/11: TtrpC KOD PCR amplification</p></li>
+
<li><p style="font-size: 18px;">9/11: TtrpC KOD PCR amplification</p></li>
+
<li><p style="font-size: 18px;">9/11: pBAR_PgpdA_EL222_TtrpC containing culture used in 3 in 1</p></li>
+
<li><p style="font-size: 18px;">9/11: pBAR_KR transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">9/11: pBAR_KR transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">9/12: pBAR_KR performed plasmid extraction and plasmid PCR (successful)</p></li>
+
<li><p style="font-size: 18px;">9/12: pBAR_PgpdA_EL222_TtrpC checked with restriction digestion</p></li>
+
<li><p style="font-size: 18px;">9/12: pBAR_PgpdA_EL222_TtrpC amplified with plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">9/12: Successfully constructed the plasmid pBAR_PgpdA_EL222_TtrpC</p></li>
+
<li><p style="font-size: 18px;">9/12: Standard part PgpdA mutation PCR (mutated PstI)</p></li>
+
<li><p style="font-size: 18px;">9/12: Standard part PMCL1 amplification PCR with KOD polymerase</p></li>
+
<li><p style="font-size: 18px;">9/13: Standard Part PMCL1 mutation PCR (mutated SpeI) </p></li>
+
<li><p style="font-size: 18px;">9/13: Standard part TtrpC amplification PCR with KOD polymerase</p></li>
+
<li><p style="font-size: 18px;">9/13: pBAR _RFP_TtrpC transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">9/13: RFP_TtrpC PCR to amplify the target sequence</p></li>
+
<li><p style="font-size: 18px;">9/13: pBAR _RFP_TtrpC did 3 in 1</p></li>
+
<li><p style="font-size: 18px;">9/13: pBAR _RFP_TtrpC digestion check</p></li>
+
<li><p style="font-size: 18px;">9/14: pBAR _RFP_TtrpC plasmid extraction</p></li>
+
<li><p style="font-size: 18px;">9/14: RFP_TtrpC digested</p></li>
+
<li><p style="font-size: 18px;">9/14: K118400 and TtrpC used PCR to amplify the target sequence</p></li>
+
<li><p style="font-size: 18px;">9/14: KR_TtrpC used PCR to amplify the target sequence</p></li>
+
<li><p style="font-size: 18px;">9/15: KR_TtrpC digested with restriction enzymes</p></li>
+
<li><p style="font-size: 18px;">9/15: Standard part TtrpC mutation PCR (mutated XbaI)</p></li>
+
<li><p style="font-size: 18px;">9/15: pBARGPE1 digested for pBAR_KR_TtrpC construction</p></li>
+
<li><p style="font-size: 18px;">9/16: pBAR_KR_TtrpC transformed into competent cell</p></li>
+
<li><p style="font-size: 18px;">9/16: Transformed pBAR_KR_TtrpC into competent cell</p></li>
+
<li><p style="font-size: 18px;">9/16: Digested pBAR_KR for transforming into Metarhizium anisopliae</p></li>
+
<li><p style="font-size: 18px;">9/16: Extracted plasmid BBa_K118400</p></li>
+
<li><p style="font-size: 18px;">9/16: pBAR_EL222_TtrpC did plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">9/16: pBAR_EL222_TtrpC did plasmid PCR (confirmed successfully)</p></li>
+
<li><p style="font-size: 18px;">9/16: pBAR _RFP_TtrpC did digestion check</p></li>
+
<li><p style="font-size: 18px;">9/17: pBAR_RFP_TtrpC did digestion check</p></li>
+
<li><p style="font-size: 18px;">9/17: pBAR_EL222_TtrpC plasmid stored and transformed cultures cryopreserved</p></li>
+
<li><p style="font-size: 18px;">9/17: pBAR_KR_TtrpC did 3 in 1</p></li>
+
<li><p style="font-size: 18px;">9/17: Extracted plasmid pBAR_KR_TtrpC</p></li>
+
  
 
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<div class="technology">Week14</div>
+
<div class="technology">9/23</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">9/18: Transformed pBAR_RFP_TtrpC into competent cell</p></li>
+
<li><p style="font-size: 16px;">Producing new feeding box which is larger and ventilation, and design the experimental boxes for Experiment 2: Infecting B. dorsalis with non-designed M. anisopliae.</p></li>
<li><p style="font-size: 18px;">9/18: pBAR_RFP_TtrpC did 3 in 1</p></li>
+
 
<li><p style="font-size: 18px;">9/18: pBAR_KR_TtrpC did plasmid PCR and digestion check</p></li>
+
<div class="imageimage">
<li><p style="font-size: 18px;">9/18: BBa_E0040 did plasmid PCR</p></li>
+
<div style="position:relative; width:48%;">
<li><p style="font-size: 18px;">9/19: Amplified GFP from plasmid BBa_E0040</p></li> 
+
<img src="https://static.igem.org/mediawiki/2016/9/91/T--NYMU-Taipei--photo-OFF-related-14697029_120300000683154255_1538186769_n.jpg" width="100%" /></div>
<li><p style="font-size: 18px;">9/19: Extracted plasmid BBa_E0040 </p></li>
+
<div style="position:relative; width:48%;">
<li><p style="font-size: 18px;">9/20: KR_TtrpC digestion</p></li>
+
<img src="https://static.igem.org/mediawiki/2016/3/30/T--NYMU-Taipei--photo-OFF-related-14699699_120300000675475754_434414381_n.jpg" width="100%" /></div>
<li><p style="font-size: 18px;">9/20: Transformed pBAR_KR_TtrpC into competent cell</p></li>
+
</div>
<li><p style="font-size: 18px;">9/20: pBAR_KR_TtrpC did 3 in 1</p></li>
+
 
<li><p style="font-size: 18px;">9/20: Extracted plasmid pBAR_KR_TtrpC </p></li>
+
<p style="font-size: 16px;">(Left picture: experimental boxes; Right picture: the internal space of feeding box)</p>
<li><p style="font-size: 18px;">9/20: pBAR_KR_TtrpC did digestion check</p></li>
+
<li><p style="font-size: 18px;">9/20: Extracted plasmid pBAR_RFP_TtrpC </p></li>
+
<li><p style="font-size: 18px;">9/20: pBAR_RFP_TtrpC did digestion check</p></li>
+
<li><p style="font-size: 18px;">9/20: RFP_TtrpC digestion</p></li>
+
<li><p style="font-size: 18px;">9/21: pBAR_KR_TtrpC did digestion check</p></li>
+
<li><p style="font-size: 18px;">9/21: pBAR_RFP_TtrpC did digestion check</p></li>
+
<li><p style="font-size: 18px;">9/21: pBAR_RFP_TtrpC did 2 in 1</p></li>
+
<li><p style="font-size: 18px;">9/21: pBARGPE1 and RFP_TtrpC digestion</p></li>
+
<li><p style="font-size: 18px;">9/22: Amplified RFP_TtrpC with KOD polymerase</p></li>
+
<li><p style="font-size: 18px;">9/22: Extracted plasmid pBAR_KR_TtrpC </p></li>
+
<li><p style="font-size: 18px;">9/22: pBAR_KR_TtrpC did plasmid PCR</p></li>
+
<li><p style="font-size: 18px;">9/22: pMCL1 and pBAR_KR_TtrpC digestion (pMCL1 was not digested successfully)</p></li>
+
<li><p style="font-size: 18px;">9/22: pBAR_PgpdA_EL222_TtrpC digested for transforming into Metarhizium anisopliae </p></li>
+
<li><p style="font-size: 18px;">9/23: Amplified pMCL1 with KOD polymerase</p></li>
+
<li><p style="font-size: 18px;">9/24: pBAR_RFP_TtrpC did digestion check</p></li>
+
<li><p style="font-size: 18px;">9/24: Extracted plasmid pBAR_RFP_TtrpC (from 9/5 plate)</p></li>
+
  
 
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<div class="technology">Week15</div>
+
<div class="technology">9/30</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">9/25: Transformed pBAR_RFP_TtrpC into competent cell</p></li>
+
<li><p style="font-size: 16px;">The new oriental fruit flies broke through cocoon in the new feeding box</p></li>
<li><p style="font-size: 18px;">9/25: RFP_TtrpC digestion</p></li>
+
 
<li><p style="font-size: 18px;">9/25: Amplified RFP-TtrpC with KOD polymerase </p></li>
+
<p style="font-size: 18px;">the new way for feeding oriental fruit flies is using gauze to be the windows that could be ventilation, and we can put watered agar and artificial feed on the top of gauze, then there were no water and feed in the box which lead to the environment being mess, and they also could have enough water and feed.</p>
<li><p style="font-size: 18px;">9/25: Amplified RFP_TtrpC with KOD polymerase</p></li>
+
<br />
<li><p style="font-size: 18px;">9/25: pMCL1 and pBAR_KR_TtrpC digestion</p></li>
+
<li><p style="font-size: 16px;">Infecting B. dorsalis with non-designed M. anisopliae started to conduct.</p></li>
<li><p style="font-size: 18px;">9/25: Transformed pBAR_pMCL1_KR_TtrpC into competent cell</p></li>
+
 
<li><p style="font-size: 18px;">9/25: Transformed pBAR_pMCL1_KR_TtrpC into competent cell</p></li>
+
<div class="imageimage">
<li><p style="font-size: 18px;">9/25: pBAR_pMCL1_KR_TtrpC did 3 in 1</p></li>
+
<div style="position:relative; width:48%;">
<li><p style="font-size: 18px;">9/26: Extracted plasmid pBAR_pMCL1_KR_TtrpC</p></li>
+
<img src="https://static.igem.org/mediawiki/2016/c/c5/T--NYMU-Taipei--photo-OFF-related-14696875_120300000677699020_204079543_n.jpg" width="100%" /></div>
<li><p style="font-size: 18px;">9/26: pBAR_RFP_TtrpC did 2 in 1</p></li>
+
<div style="position:relative; width:48%;">
<li><p style="font-size: 18px;">9/26: Extracted plasmid pBAR_RFP_TtrpC </p></li>
+
<img src="https://static.igem.org/mediawiki/2016/4/46/T--NYMU-Taipei--photo-OFF-related-14696862_120300000674829370_219600743_n.jpg" width="100%" /></div>
<li><p style="font-size: 18px;">9/26: pBAR_RFP_TtrpC did digestion check</p></li>
+
</div>
<li><p style="font-size: 18px;">9/26: pBAR_RFP_TtrpC did digestion check</p></li>
+
<br />
<li><p style="font-size: 18px;">9/26: Amplified pMCL1 with KOD polymerase</p></li>
+
<div class="imageimage">
<li><p style="font-size: 18px;">9/27: Amplified pMCL1 with KOD polymerase </p></li>
+
<div style="position:relative; width:48%;">
<li><p style="font-size: 18px;">9/28: pBAR_pMCL1_KR_TtrpC did digestion check</p></li>
+
<img src="https://static.igem.org/mediawiki/2016/b/b9/T--NYMU-Taipei--photo-OFF-related-14686253_120300000675039507_1525612271_n.jpg" width="100%" /></div>
<li><p style="font-size: 18px;">9/28: pBAR_RFP_TtrpC did plasmid PCR</p></li>
+
<div style="position:relative; width:48%;">
<li><p style="font-size: 18px;">9/28: Successfully constructed the plasmid pBAR_RFP_TtrpC</p></li>  
+
<img src="https://static.igem.org/mediawiki/2016/c/c7/T--NYMU-Taipei--photo-OFF-related-14627961_120300000679852339_2089167734_n.jpg" width="100%" /></div>
<li><p style="font-size: 18px;">9/29: Amplified pMCL1 with KOD polymerase</p></li>
+
</div>
<li><p style="font-size: 18px;">9/30: pBAR_pMCL1_KR_TtrpC did digestion check</p></li>
+
 
<li><p style="font-size: 18px;">9/30: Received the junction primer of GFP-TtrpC</p></li>
+
<p style="font-size: 16px;">Photos shows three concentration condition and negative control environment of experiment "Infecting B. dorsalis with non-designed M. anisopliae"</p>
<li><p style="font-size: 18px;">9/30: GFP_TtrpC ran ligation PCR</p></li>
+
<li><p style="font-size: 18px;">10/1: GFP_TtrpC ran ligation PCR</p></li>
+
  
 
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<div class="technology">Week16</div>
+
<div class="technology">10/1</div>
 
<div class="thelanguage">
 
<div class="thelanguage">
<li><p style="font-size: 18px;">10/2: GFP_TtrpC digested for ligation with pBARGPE1 </p></li>
+
<li><p style="font-size: 16px;">Keeping on Experiment 2-1 (9/30~10/7)</p></li>
<li><p style="font-size: 18px;">10/2: Transformed pBAR_GFP_TtrpC into competent cells</p></li>
+
<li><p style="font-size: 18px;">10/2: pBARGPE1 digested for pBAR_GFP_TtrpC construction</p></li>
+
<li><p style="font-size: 18px;">10/2: pBARGPE1 resuspended (from cryopreservation)</p></li>
+
<li><p style="font-size: 18px;">10/3: Extracted plasmid pBARGPE1</p></li>
+
<li><p style="font-size: 18px;">10/3: pBAR_GFP_TtrpC containing cultures used in 2 in 1</p></li>
+
<li><p style="font-size: 18px;">10/3: Extracted plasmid pBAR_GFP_TtrpC</p></li>
+
<li><p style="font-size: 18px;">10/3: pBAR_GFP_TtrpC digestion check(failure)</p></li>
+
<li><p style="font-size: 18px;">10/3: pBAR_GFP_TtrpC PCR check(failure)</p></li>
+
<li><p style="font-size: 18px;">10/3: Transformed pBAR_GFP_TtrpC into competent cells</p></li>
+
<li><p style="font-size: 18px;">10/3: pBARGPE1 checked with restriction digestion (correct)</p></li>
+
<li><p style="font-size: 18px;">10/4: pBARGPE1 plasmid stored</p></li>
+
<li><p style="font-size: 18px;">10/4: pBAR_GFP_TtrpC containing cultures used in 2 in 1</p></li>
+
<li><p style="font-size: 18px;">10/4: pBAR_GFP_TtrpC plasmid extraction</p></li>
+
<li><p style="font-size: 18px;">10/4: pBAR_GFP_TtrpC digestion check</p></li>
+
  
 
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+
<div class="technology">10/7</div>
 +
<div class="thelanguage">
 +
<li><p style="font-size: 16px;">Experiment 2-1 finished.</p></li>
 +
 
 +
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</div>
 +
 
 +
<div class="technology">10/10</div>
 +
<div class="thelanguage">
 +
<p style="font-size: 16px;">Experiment 2-2 "infecting female B. dorsalis by copulation with infected male B. dorsalis" started to conduct.</p>
 +
 
 +
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</div>
 +
 
 +
<div id="wrap">
 +
 
 +
<div class="fund" style="white-space: pre-wrap;">
 +
 
 +
<h2 style="margin-top:30px; margin-bottom:10px;">Q&A Section</h2><hr />
 +
 
 +
<p style="font-size:16px;">How to CULTURE oriental fruit flies?</p>
 +
<p style="font-size:16px;"> The oriental fruit flies can grow in a transparent large container and centrifuge tubes with a piece of cotton placed at the opening to prevent them from escaping while still allowing air exchange.</p>
 +
<p style="font-size:16px;"> Feeding on sucrose-peptone agar (sited by ATCC) when you choose the centrifuge tubes as their living environment; a ratio of composition below is the way to feed the fruit flies in a larger container. The larval need the other formula to grow up whether living in the centrifuge tubes or the larger transparent container. The adult feeding formula without peptone can also alive the oriental fruit flies but not breeding.</p>
 +
<p style="font-size:16px;">Larva formula                                           
 +
Yeast extraction 35g
 +
Sucrose 60g
 +
Oat                 120g
 +
Sodium benzoate 1g
 +
Hydrochloric acid 4.5ml, 37%
 +
Water 450ml
 +
 
 +
Adult formula ratio
 +
Sucrose: yeast extraction: peptone
 +
3:1:1
 +
</p>
 +
<p style="font-size:16px;"> The advantage of cultivating in large container is avoiding the tight space that oriental fruit flies can almost only walk and then causing the growth medium spoil easily. On the other hand, cultivating the fruit flies in the centrifuge tubes can easily distinguish the situation of the oriental fruit flies, for example, gender, health, quantity to take the correct actions.</p>
 +
<p style="font-size:16px;">How to prevent COMTAMINATION?</p>
 +
<li><p style="font-size:16px;"></p>Adding preservatives, for instance, sodium benzoate, and decreasing environmental humidity can decease the growth of the mold on agar.</li>
 +
<li><p style="font-size:16px;"></p>Sterilize cotton according common lab procedure or just buy pre-sterilized one.</li><br />
 +
<p style="font-size:16px;">How do you KEEP the oriental fruit flies in place during experiments?</p>
 +
<li><p style="font-size:16px;"></p>Using carbon dioxide gas to induce comatose and try your best to contain the gas within the tube and the oriental fruit flies should be unconscious after 10-20 seconds.</li>
 +
<li><p style="font-size:16px;"></p>Induce coma under low temperature.</li><br />
 +
<p style="font-size:16px;">How about the methyl eugenol? Are there any suggestions on attracting the male oriental fruit flies or the actual situation that farmer using it to prevent the oriental fruit fly pest?</p>
 +
<li><p style="font-size:16px;">It is best to complete experiments using methyl eugenol before 2:00 PM.</p></li>
 +
<li><p style="font-size:16px;">Several time experiments may cause the male oriental fruit flies became desensitized to methyl eugenol, so it's important to change the sample you test on the experiments routinely to avoid the factor to interfere the result.</p></li>
 +
<li><p style="font-size:16px;">The attraction traps putting in the orchard need to add pure and undiluted methyl eugenol to capture the oriental fruit flies. It also needs some cottons or gauzes to separate the oriental fruit flies and methyl eugenol to prevent the chain of fruit flies and eventually causing the death.</p></li>
 +
<li><p style="font-size:16px;">It's not a good idea to set the trap when (a) it's a rainy day (b) it's not the harvest season of the guava or tangerine, or the number of the fruit flies captured will not high.</p></li><br />
 +
<p style="font-size:16px;">Is the common characteristic among the hemolymph of Bactrocera dorsalis and other insects sufficiently confirmed the accuracy of the experiment result?</p><br />
 +
<p style="font-size:16px;">Can the designed M. anisopliae actually invade B. dorsalis?</p>
 +
 
 +
</div>
 +
 
 +
<div class="fund" style="white-space: pre-wrap;">
 +
 
 +
<h2 style="margin-top:30px; margin-bottom:10px;">Acknowledgements</h2><hr />
 +
 
 +
<p style="font-size:16px;">Beitou orchard
 +
S. J. Chen Grower
 +
</p>
 +
<p style="font-size:16px;">Beitou orchard
 +
Z. L. Liao Grower
 +
</p>
 +
<p style="font-size:16px;">Bioresource Collection and Research Center
 +
G. Y. Liou Fellow
 +
</p>
 +
<p style="font-size:16px;">Chiayi Agricultural Experiment Branch
 +
P. H. Chen Research assistant
 +
</p>
 +
<p style="font-size:16px;">Kaohsiung District Agricultural Research and Extension Station, COA, EY
 +
M. N. Tseng Research director
 +
</p>
 +
<p style="font-size:16px;">National Chung Hsing University, the Department of Entomology
 +
S. Y. Hwang Professor
 +
</p>
 +
<p style="font-size:16px;">National Chung Hsing University, the Department of Entomology
 +
Y. Y. Tseng Research assistant
 +
</p>
 +
<p style="font-size:16px;">Taiwan Agricultural Research Institute, Applied Zoology Division
 +
M. Y. Chiang Research assistant
 +
</p>
 +
<p style="font-size:16px;">Taiwan Agricultural Research Institute, Applied Zoology Division
 +
Y. B. Huang Professor
 +
/p>
 +
 
 +
</div>
 +
</div>
 +
 
 +
<script>if (window.runOnloadHook) runOnloadHook();</script></div>
 +
 
  
 
</body>
 
</body>
 
</html>
 
</html>

Latest revision as of 20:13, 19 October 2016

Overview


This section of our wiki contains the protocols for our insect experiments, including cultivation, infection rate tests, and hemolymph extraction.

Related experiment schedule & Lab note



Experiments

                                       
Experiments related to B. dorsalisNumberDate
Diameter of the tunnel that allows passage to one B. dorsalis18/30~9/1
Infecting B. dorsalis with non-designed M. anisopliae2-19/30~10/7
infecting female B. dorsalis by copulation with infected male B. dorsalis2-210/10~10/17
                                       
Experiments related to B. dorsalisNumberDate
Diameter of the tunnel that allows passage to one B. dorsalis18/30~9/1
Infecting B. dorsalis with non-designed M. anisopliae2-19/30~10/7
infecting female B. dorsalis by copulation with infected male B. dorsalis2-210/10~10/17
                                       
Experiments about hemolymph extractionNumberDate
Blatta lateralis19/20~9/30
Bactrocera dorsalis29/29~10/5
Bombyx mori310/3~10/
                                       
Experiments about hemolymph extractionNumberDate
Blatta lateralis19/20~9/30
Bactrocera dorsalis29/29~10/5
Bombyx mori310/3~10/

Routine works

                       
Routine tasks of feeding Bactrocera dorsalisDate
Produce & change the tube with the specific agar8/24~9/20
Produce & change water gel and the specific ratio fodder9/22~10/
                       
Routine tasks of feeding Bactrocera dorsalisDate
Produce & change the tube with the specific agar8/24~9/20
Produce & change water gel and the specific ratio fodder9/22~10/
                       
Routine tasks of hemolymph extractionDate
Collect the mulberry leaves to feed the silkworm10/3~10/
Sterilize the related equipments9/20~10/
                       
Routine tasks of hemolymph extractionDate
Collect the mulberry leaves to feed the silkworm10/3~10/
Sterilize the related equipments9/20~10/


8/23
  • Oriental fruit flies sent to lab and cultivated by large transparent box to avoid oriental fruit flies flying out.

  • [Collapse]

    8/24
  • We used both of centrifuge tube and feeding box to feed oriental fruit flies for comparing and ensuring the status of oriental fruit flies that established the independent space for observing oriental fruit flies.


  • [Collapse]

    8/25
  • B. dorsalis started to break through the cocoon. We conducted to put B. dorsalis to centrifuge tubes, avoiding the feeding box cannot load all oriental fruit flies. We poured the special agar to centrifuge tubes, and put centrifuges into entrance to catch oriental fruit flies. Then we sealed the centrifuge tubes by cotton.

  • (The team members put agar into centrifuge tubes which would be their feed.)

    (The left picture is that oriental fruit flies broke through cocoon; the right picture is the feeding box & centrifuge tubes where fed oriental fruit flies.)

    [Collapse]

    8/30
  • First time to Conducting Experiment 1

  • [Collapse]

    9/3
  • Changing the centrifuge tubes where oriental fruit flies lived. (Avoid the environment being mess.) /p>

  • [Collapse]

    9/5
  • Changing the centrifuge tubes where oriental fruit flies lived.

  • [Collapse]

    9/6
  • The oriental fruit flies in centrifuge tubes are dead quickly, so we conducted trouble shooting and sent the mail to professors who research oriental fruit flies.

  • We took the trap to Beitou orchard to try to catch oriental fruit flies.

  • [Collapse]

    9/7
  • Second time to Conducting Experiment 1.

  • Conducting trouble shooting.

  • [Collapse]

    9/10
  • Searching the store selling the silkworm for extracting hemolymph which is used to induce pMcl1.

  • [Collapse]

    9/13
  • Visiting two farmers working in the orchard to ask the information about oriental fruit flies in the nature environment, and installing the trap of catching oriental fruit flies.

  • (Left picture: the team member install the trap; Right picture: the farmer and our team member took a picture)

  • Sent the mail to researchers to ask for making public the content of the mail.

  • [Collapse]

    9/15
  • Communicating with Chang Ming ecological education sericulture, asking the information of buying silkworm.

  • [Collapse]

    9/16
  • Picking up the oriental fruit fly larval from rotten guavas and feeding them.

  • Left picture: the team members were picking up the oriental fruit fly larval from rotten guavas; Right picture: the larval have picked up and put into another box. Expected becoming pupae after six days.

  • [Collapse]

    9/22
  • For the situation that our fruit flies in the centrifuge tubes were dead quickly , so we visited Dr. Yu-Bing Huang in Taiwan Agricultural Research Institute, Applied Zoology Division, and asking the problems about the right way for feeding oriental fruit flies. We change our way of feeding oriental fruit flies.

  • [Collapse]

    9/23
  • Producing new feeding box which is larger and ventilation, and design the experimental boxes for Experiment 2: Infecting B. dorsalis with non-designed M. anisopliae.

  • (Left picture: experimental boxes; Right picture: the internal space of feeding box)

    [Collapse]

    9/30
  • The new oriental fruit flies broke through cocoon in the new feeding box

  • the new way for feeding oriental fruit flies is using gauze to be the windows that could be ventilation, and we can put watered agar and artificial feed on the top of gauze, then there were no water and feed in the box which lead to the environment being mess, and they also could have enough water and feed.


  • Infecting B. dorsalis with non-designed M. anisopliae started to conduct.


  • Photos shows three concentration condition and negative control environment of experiment "Infecting B. dorsalis with non-designed M. anisopliae"

    [Collapse]

    10/1
  • Keeping on Experiment 2-1 (9/30~10/7)

  • [Collapse]

    10/7
  • Experiment 2-1 finished.

  • [Collapse]

    10/10

    Experiment 2-2 "infecting female B. dorsalis by copulation with infected male B. dorsalis" started to conduct.

    [Collapse]

    Q&A Section


    How to CULTURE oriental fruit flies?

    The oriental fruit flies can grow in a transparent large container and centrifuge tubes with a piece of cotton placed at the opening to prevent them from escaping while still allowing air exchange.

    Feeding on sucrose-peptone agar (sited by ATCC) when you choose the centrifuge tubes as their living environment; a ratio of composition below is the way to feed the fruit flies in a larger container. The larval need the other formula to grow up whether living in the centrifuge tubes or the larger transparent container. The adult feeding formula without peptone can also alive the oriental fruit flies but not breeding.

    Larva formula Adult formula ratio Yeast extraction 35g Sucrose: yeast extraction: peptone Sucrose 60g 3:1:1 Oat 120g Sodium benzoate 1g Hydrochloric acid 4.5ml, 37% Water 450ml

    The advantage of cultivating in large container is avoiding the tight space that oriental fruit flies can almost only walk and then causing the growth medium spoil easily. On the other hand, cultivating the fruit flies in the centrifuge tubes can easily distinguish the situation of the oriental fruit flies, for example, gender, health, quantity to take the correct actions.

    How to prevent COMTAMINATION?

  • Adding preservatives, for instance, sodium benzoate, and decreasing environmental humidity can decease the growth of the mold on agar.
  • Sterilize cotton according common lab procedure or just buy pre-sterilized one.

  • How do you KEEP the oriental fruit flies in place during experiments?

  • Using carbon dioxide gas to induce comatose and try your best to contain the gas within the tube and the oriental fruit flies should be unconscious after 10-20 seconds.
  • Induce coma under low temperature.

  • How about the methyl eugenol? Are there any suggestions on attracting the male oriental fruit flies or the actual situation that farmer using it to prevent the oriental fruit fly pest?

  • It is best to complete experiments using methyl eugenol before 2:00 PM.

  • Several time experiments may cause the male oriental fruit flies became desensitized to methyl eugenol, so it's important to change the sample you test on the experiments routinely to avoid the factor to interfere the result.

  • The attraction traps putting in the orchard need to add pure and undiluted methyl eugenol to capture the oriental fruit flies. It also needs some cottons or gauzes to separate the oriental fruit flies and methyl eugenol to prevent the chain of fruit flies and eventually causing the death.

  • It's not a good idea to set the trap when (a) it's a rainy day (b) it's not the harvest season of the guava or tangerine, or the number of the fruit flies captured will not high.


  • Acknowledgements


    Beitou orchard S. J. Chen Grower

    Beitou orchard Z. L. Liao Grower

    Bioresource Collection and Research Center G. Y. Liou Fellow

    Chiayi Agricultural Experiment Branch P. H. Chen Research assistant

    Kaohsiung District Agricultural Research and Extension Station, COA, EY M. N. Tseng Research director

    National Chung Hsing University, the Department of Entomology S. Y. Hwang Professor

    National Chung Hsing University, the Department of Entomology Y. Y. Tseng Research assistant

    Taiwan Agricultural Research Institute, Applied Zoology Division M. Y. Chiang Research assistant

    Taiwan Agricultural Research Institute, Applied Zoology Division Y. B. Huang Professor /p>

    Overview


    This section of our wiki contains the protocols for our insect experiments, including cultivation, infection rate tests, and hemolymph extraction.

    Related experiment schedule & Lab note


    Experiments

                                           
    Experiments related to B. dorsalisNumberDate
    Diameter of the tunnel that allows passage to one B. dorsalis18/30~9/1
    Infecting B. dorsalis with non-designed M. anisopliae2-19/30~10/7
    infecting female B. dorsalis by copulation with infected male B. dorsalis2-210/10~10/17
                                           
    Experiments about hemolymph extractionNumberDate
    Blatta lateralis19/20~9/30
    Bactrocera dorsalis29/29~10/5
    Bombyx mori310/3~10/

    Routine works

                           
    Routine tasks of feeding Bactrocera dorsalisDate
    Produce & change the tube with the specific agar8/24~9/20
    Produce & change water gel and the specific ratio fodder9/22~10/
                           
    Routine tasks of hemolymph extractionDate
    Collect the mulberry leaves to feed the silkworm10/3~10/
    Sterilize the related equipments9/20~10/


    8/23
  • Oriental fruit flies sent to lab and cultivated by large transparent box to avoid oriental fruit flies flying out.

  • [Collapse]

    8/24
  • We used both of centrifuge tube and feeding box to feed oriental fruit flies for comparing and ensuring the status of oriental fruit flies that established the independent space for observing oriental fruit flies.


  • [Collapse]

    8/25
  • B. dorsalis started to break through the cocoon. We conducted to put B. dorsalis to centrifuge tubes, avoiding the feeding box cannot load all oriental fruit flies. We poured the special agar to centrifuge tubes, and put centrifuges into entrance to catch oriental fruit flies. Then we sealed the centrifuge tubes by cotton.

  • (The team members put agar into centrifuge tubes which would be their feed.)

    (The left picture is that oriental fruit flies broke through cocoon; the right picture is the feeding box & centrifuge tubes where fed oriental fruit flies.)

    [Collapse]

    8/30
  • First time to Conducting Experiment 1

  • [Collapse]

    9/3
  • Changing the centrifuge tubes where oriental fruit flies lived. (Avoid the environment being mess.) /p>

  • [Collapse]

    9/5
  • Changing the centrifuge tubes where oriental fruit flies lived.

  • [Collapse]

    9/6
  • The oriental fruit flies in centrifuge tubes are dead quickly, so we conducted trouble shooting and sent the mail to professors who research oriental fruit flies.

  • We took the trap to Beitou orchard to try to catch oriental fruit flies.

  • [Collapse]

    9/7
  • Second time to Conducting Experiment 1.

  • Conducting trouble shooting.

  • [Collapse]

    9/10
  • Searching the store selling the silkworm for extracting hemolymph which is used to induce pMcl1.

  • [Collapse]

    9/13
  • Visiting two farmers working in the orchard to ask the information about oriental fruit flies in the nature environment, and installing the trap of catching oriental fruit flies.

  • (Left picture: the team member install the trap; Right picture: the farmer and our team member took a picture)

  • Sent the mail to researchers to ask for making public the content of the mail.

  • [Collapse]

    9/15
  • Communicating with Chang Ming ecological education sericulture, asking the information of buying silkworm.

  • [Collapse]

    9/16
  • Picking up the oriental fruit fly larval from rotten guavas and feeding them.

  • Left picture: the team members were picking up the oriental fruit fly larval from rotten guavas; Right picture: the larval have picked up and put into another box. Expected becoming pupae after six days.

  • [Collapse]

    9/22
  • For the situation that our fruit flies in the centrifuge tubes were dead quickly , so we visited Dr. Yu-Bing Huang in Taiwan Agricultural Research Institute, Applied Zoology Division, and asking the problems about the right way for feeding oriental fruit flies. We change our way of feeding oriental fruit flies.

  • [Collapse]

    9/23
  • Producing new feeding box which is larger and ventilation, and design the experimental boxes for Experiment 2: Infecting B. dorsalis with non-designed M. anisopliae.

  • (Left picture: experimental boxes; Right picture: the internal space of feeding box)

    [Collapse]

    9/30
  • The new oriental fruit flies broke through cocoon in the new feeding box

  • the new way for feeding oriental fruit flies is using gauze to be the windows that could be ventilation, and we can put watered agar and artificial feed on the top of gauze, then there were no water and feed in the box which lead to the environment being mess, and they also could have enough water and feed.


  • Infecting B. dorsalis with non-designed M. anisopliae started to conduct.


  • Photos shows three concentration condition and negative control environment of experiment "Infecting B. dorsalis with non-designed M. anisopliae"

    [Collapse]

    10/1
  • Keeping on Experiment 2-1 (9/30~10/7)

  • [Collapse]

    10/7
  • Experiment 2-1 finished.

  • [Collapse]

    10/10

    Experiment 2-2 "infecting female B. dorsalis by copulation with infected male B. dorsalis" started to conduct.

    [Collapse]

    Q&A Section


    How to CULTURE oriental fruit flies?

    The oriental fruit flies can grow in a transparent large container and centrifuge tubes with a piece of cotton placed at the opening to prevent them from escaping while still allowing air exchange.

    Feeding on sucrose-peptone agar (sited by ATCC) when you choose the centrifuge tubes as their living environment; a ratio of composition below is the way to feed the fruit flies in a larger container. The larval need the other formula to grow up whether living in the centrifuge tubes or the larger transparent container. The adult feeding formula without peptone can also alive the oriental fruit flies but not breeding.

    Larva formula Yeast extraction 35g Sucrose 60g Oat 120g Sodium benzoate 1g Hydrochloric acid 4.5ml, 37% Water 450ml Adult formula ratio Sucrose: yeast extraction: peptone 3:1:1

    The advantage of cultivating in large container is avoiding the tight space that oriental fruit flies can almost only walk and then causing the growth medium spoil easily. On the other hand, cultivating the fruit flies in the centrifuge tubes can easily distinguish the situation of the oriental fruit flies, for example, gender, health, quantity to take the correct actions.

    How to prevent COMTAMINATION?

  • Adding preservatives, for instance, sodium benzoate, and decreasing environmental humidity can decease the growth of the mold on agar.
  • Sterilize cotton according common lab procedure or just buy pre-sterilized one.

  • How do you KEEP the oriental fruit flies in place during experiments?

  • Using carbon dioxide gas to induce comatose and try your best to contain the gas within the tube and the oriental fruit flies should be unconscious after 10-20 seconds.
  • Induce coma under low temperature.

  • How about the methyl eugenol? Are there any suggestions on attracting the male oriental fruit flies or the actual situation that farmer using it to prevent the oriental fruit fly pest?

  • It is best to complete experiments using methyl eugenol before 2:00 PM.

  • Several time experiments may cause the male oriental fruit flies became desensitized to methyl eugenol, so it's important to change the sample you test on the experiments routinely to avoid the factor to interfere the result.

  • The attraction traps putting in the orchard need to add pure and undiluted methyl eugenol to capture the oriental fruit flies. It also needs some cottons or gauzes to separate the oriental fruit flies and methyl eugenol to prevent the chain of fruit flies and eventually causing the death.

  • It's not a good idea to set the trap when (a) it's a rainy day (b) it's not the harvest season of the guava or tangerine, or the number of the fruit flies captured will not high.


  • Is the common characteristic among the hemolymph of Bactrocera dorsalis and other insects sufficiently confirmed the accuracy of the experiment result?


    Can the designed M. anisopliae actually invade B. dorsalis?

    Acknowledgements


    Beitou orchard S. J. Chen Grower

    Beitou orchard Z. L. Liao Grower

    Bioresource Collection and Research Center G. Y. Liou Fellow

    Chiayi Agricultural Experiment Branch P. H. Chen Research assistant

    Kaohsiung District Agricultural Research and Extension Station, COA, EY M. N. Tseng Research director

    National Chung Hsing University, the Department of Entomology S. Y. Hwang Professor

    National Chung Hsing University, the Department of Entomology Y. Y. Tseng Research assistant

    Taiwan Agricultural Research Institute, Applied Zoology Division M. Y. Chiang Research assistant

    Taiwan Agricultural Research Institute, Applied Zoology Division Y. B. Huang Professor /p>