http://2013.igem.org/wiki/index.php?title=Team:NCTU_Formosa/index&feed=atom&action=historyTeam:NCTU Formosa/index - Revision history2024-03-29T04:48:14ZRevision history for this page on the wikiMediaWiki 1.16.5http://2013.igem.org/wiki/index.php?title=Team:NCTU_Formosa/index&diff=122851&oldid=prevCalvinhue at 04:40, 14 September 20132013-09-14T04:40:36Z<p></p>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del class="diffchange diffchange-inline">class="team">by NCTU_Formosa<</del>/<del class="diffchange diffchange-inline">span><div class="wordbox"><p>We have proven a sRNA-regulated system of our own to be an effective and competent way for regulating gene expressions. <</del>/<del class="diffchange diffchange-inline">p></del></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div></<ins class="diffchange diffchange-inline">head</ins>></div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del class="diffchange diffchange-inline"><p>Recent studies have shown that sRNA-mediated regulation is an important factor to bacterial growth. sRNAs work by base pairing with limited or extended complementary target mRNAs, regulating protein productions. Using sRNA mechanism, we can control gene expression in RNA level, in contrast to common promoters that functions on DNA level. Since the existing sRNAs in Escherishia Coli have important functions in other metabolic processes, we designed an artificial sRNA with high specificity to avoid undesired base binding in vitro.<</del>/<del class="diffchange diffchange-inline">p></del></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div></div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del class="diffchange diffchange-inline"><p>By using the sRNA-regulated system, red light induced ooperator, and thirty seven degree Celsius ribosome binding site (RBS), we constructed a manipulatable system that is capable of expressing four different genes under different conditions</del>. <del class="diffchange diffchange-inline">In other words, it is a multitask machine</del>.<del class="diffchange diffchange-inline"><</del>/<del class="diffchange diffchange-inline">p><</del>/<del class="diffchange diffchange-inline">div></div></div></div></del></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div></div></td></tr>
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</table>Calvinhuehttp://2013.igem.org/wiki/index.php?title=Team:NCTU_Formosa/index&diff=121964&oldid=prevCalvinhue at 17:12, 13 September 20132013-09-13T17:12:15Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>class="team">by NCTU_Formosa</span><div class="wordbox"><p>We have proven a sRNA-regulated system of our own to be an effective and competent way for regulating gene expressions. </p></div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>class="team">by NCTU_Formosa</span><div class="wordbox"><p>We have proven a sRNA-regulated system of our own to be an effective and competent way for regulating gene expressions. </p></div></td></tr>
</table>Calvinhuehttp://2013.igem.org/wiki/index.php?title=Team:NCTU_Formosa/index&diff=94493&oldid=prevCalvinhue at 08:49, 30 August 20132013-08-30T08:49:51Z<p></p>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div>class="team">by NCTU_Formosa</span><div class="wordbox"><p>We have <del class="diffchange diffchange-inline">developed and </del>proven a sRNA-regulated system of our own to be an effective and competent </div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div>class="team">by NCTU_Formosa</span><div class="wordbox"><p>We have proven a sRNA-regulated system of our own to be an effective and competent way for regulating gene expressions. <ins class="diffchange diffchange-inline"></p></ins></div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div> </div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline"><p></ins>Recent studies have shown that sRNA-mediated regulation is an important factor to bacterial growth. sRNAs work by base pairing with limited or extended complementary target mRNAs, regulating protein productions. Using sRNA mechanism, we can control gene expression in RNA level, in contrast to common promoters that functions on DNA level. Since the existing sRNAs in Escherishia Coli have important functions in other metabolic processes, we designed an artificial sRNA with high specificity to avoid undesired base binding in vitro.<ins class="diffchange diffchange-inline"></p></ins></div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div>way for regulating gene expressions. Recent studies have shown that sRNA-mediated regulation is an important factor to bacterial growth. sRNAs work by base </div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div><ins class="diffchange diffchange-inline"><p></ins>By using the sRNA-regulated system, <ins class="diffchange diffchange-inline">red </ins>light induced <ins class="diffchange diffchange-inline">ooperator</ins>, and thirty seven degree Celsius ribosome binding site (RBS), we constructed a manipulatable <ins class="diffchange diffchange-inline">system that is capable </ins>of <ins class="diffchange diffchange-inline">expressing four different genes under different conditions. In other words</ins>, <ins class="diffchange diffchange-inline">it </ins>is a <ins class="diffchange diffchange-inline">multitask machine</ins>.</p></div></div></div></div></div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div> </div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div></div></td></tr>
<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div>pairing with limited or extended complementary target mRNAs, regulating protein productions. Using sRNA mechanism, we can control gene expression in RNA </div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div></div></td></tr>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div>level, in contrast to common promoters that functions on DNA level. Since the existing sRNAs in Escherishia Coli have important functions in other metabolic </div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div></div></td></tr>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div>processes, we designed an artificial sRNA with high specificity to avoid undesired base binding in vitro. By using the sRNA-regulated system, light induced </div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div></div></td></tr>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del class="diffchange diffchange-inline">promoter</del>, and thirty seven degree Celsius ribosome binding site (RBS), we constructed a manipulatable <del class="diffchange diffchange-inline">circuit to adjust the concentration </del>of <del class="diffchange diffchange-inline">IAA</del>, <del class="diffchange diffchange-inline">an </del></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div></div></td></tr>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div><del class="diffchange diffchange-inline">important factor for plant growth. This circuit </del>is <del class="diffchange diffchange-inline">proven to be practical in </del>a <del class="diffchange diffchange-inline">closed system of plant tissue</del>.</p></div></div></div></div></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div></div></td></tr>
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</table>Calvinhuehttp://2013.igem.org/wiki/index.php?title=Team:NCTU_Formosa/index&diff=92068&oldid=prevCalvinhue at 18:40, 28 August 20132013-08-28T18:40:16Z<p></p>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>class="team">by NCTU_Formosa</span><div class="wordbox"><p>We have developed and proven a sRNA-regulated system of our own to be an effective and competent </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>class="team">by NCTU_Formosa</span><div class="wordbox"><p>We have developed and proven a sRNA-regulated system of our own to be an effective and competent </div></td></tr>
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<tr><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>promoter, and thirty seven degree Celsius ribosome binding site (RBS), we constructed a manipulatable circuit to adjust the concentration of IAA, an </div></td><td class='diff-marker'> </td><td style="background: #eee; color:black; font-size: smaller;"><div>promoter, and thirty seven degree Celsius ribosome binding site (RBS), we constructed a manipulatable circuit to adjust the concentration of IAA, an </div></td></tr>
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<tr><td class='diff-marker'>-</td><td style="background: #ffa; color:black; font-size: smaller;"><div>important factor for plant growth. This circuit is proven to be practical in a closed system of plant tissue.</p></div></div></div></div></td><td class='diff-marker'>+</td><td style="background: #cfc; color:black; font-size: smaller;"><div>important factor for plant growth. This circuit is proven to be practical in a closed system of plant tissue.</p<ins class="diffchange diffchange-inline">></div</ins>></div></div></div></div></td></tr>
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</table>Calvinhuehttp://2013.igem.org/wiki/index.php?title=Team:NCTU_Formosa/index&diff=88729&oldid=prevCalvinhue at 16:34, 26 August 20132013-08-26T16:34:26Z<p></p>
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</table>Calvinhuehttp://2013.igem.org/wiki/index.php?title=Team:NCTU_Formosa/index&diff=88728&oldid=prevCalvinhue: Created page with "{{:Team:NCTU Formosa/source/head}} <script src="http://code.jquery.com/jquery-1.10.1.min.js"></script> <script src="stellar.js"></script> <script> $(function(){ $.stel..."2013-08-26T16:33:28Z<p>Created page with "{{:Team:NCTU Formosa/source/head}} <script src="http://code.jquery.com/jquery-1.10.1.min.js"></script> <script src="stellar.js"></script> <script> $(function(){ $.stel..."</p>
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<div id="description" class="page" data-stellar-background-ratio="0.5"><div class="box"><div class="title">E.colightuner</div><span <br />
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class="team">by NCTU_Formosa</span><div class="wordbox"><p>We have developed and proven a sRNA-regulated system of our own to be an effective and competent <br />
<br />
way for regulating gene expressions. Recent studies have shown that sRNA-mediated regulation is an important factor to bacterial growth. sRNAs work by base <br />
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pairing with limited or extended complementary target mRNAs, regulating protein productions. Using sRNA mechanism, we can control gene expression in RNA <br />
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level, in contrast to common promoters that functions on DNA level. Since the existing sRNAs in Escherishia Coli have important functions in other metabolic <br />
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processes, we designed an artificial sRNA with high specificity to avoid undesired base binding in vitro. By using the sRNA-regulated system, light induced <br />
<br />
promoter, and thirty seven degree Celsius ribosome binding site (RBS), we constructed a manipulatable circuit to adjust the concentration of IAA, an <br />
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important factor for plant growth. This circuit is proven to be practical in a closed system of plant tissue.</p></div></div></div><br />
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