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- | {{:Team:Grenoble/Templates/Biology}}
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- | <html xmlns="http://www.w3.org/1999/xhtml" xml:lang="en" lang="en">
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- | <body id="Biology">
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- | <div id="cadre">
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- | <section>
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- | <h1>August</h1>
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- | <a href="https://2012.igem.org/Team:Grenoble/Biology/Notebook/August">Week 31</a> •
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- | <a href="https://2012.igem.org/Team:Grenoble/Biology/Notebook/July/week_32">Week 32</a> •
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- | <a href="https://2012.igem.org/Team:Grenoble/Biology/Notebook/July/week_33">Week 33</a> •
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- | <a href="https://2012.igem.org/Team:Grenoble/Biology/Notebook/July/week_34">Week 34</a> •
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- | <a href="https://2012.igem.org/Team:Grenoble/Biology/Notebook/July/week_35">Week 35</a>
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- | </section>
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- | <br/>
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- | <section>
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- | <h1> Week 32: August 06<span class="exposant">th</span> to 12<span class="exposant">th</span> </h1>
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- | <h2> Goal of the week: </h2>
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- | </section>
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- | <section>
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- | <h2> Monday, August 06<span class="exposant">th</span>:</h2>
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- | We wanted to check if the Gibson Assemblies (12/08/01) worked well.<br/>
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- | <br/>
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- | To separate (<a href="https://2012.igem.org/Team:Grenoble/Biology/Protocols/Gel">protocol</a>) the GA miniprep (12/08/03) products, we prepared a 1.8% TAE agarose gel.<br/>
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- | Migration conditions = 100V during 30 min.<br/>
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- | In order to reveal the DNA fragments, we used <a href="https://2012.igem.org/Team:Grenoble/Biology/Protocols/EtBr">EtBr</a>.<br/>
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- | <br/>
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- | <center><img src="https://static.igem.org/mediawiki/2012/4/44/120806_pcr_miniprep_2.jpg" alt="photo_gel_27"/></center>
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- | <div class="legend"><p><center><u>Migration result for a 1.8% TAE agarose gel</u><br/>
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- | <i>(the DNA ladder scale is in kb)</i></center></p>
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- | <ul><li><b>Lane 1:</b> pLAC_rsmY (pSB1A3) <b>3</b> miniprep product</li>
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- | <li><b>Lane 2:</b> pLAC_rsmY (pSB1A3) <b>2</b> miniprep product</li>
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- | <li><b>Lane 3:</b> pLAC_rsmY (pSB1A3) <b>1</b> miniprep product</li>
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- | <li><b>Lane 4:</b> pLAC_fha1_eCFP (pSB4C5) <b>2</b> miniprep product</li>
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- | <li><b>Lane 5:</b> pLAC_fha1_eCFP (pSB4C5) <b>1</b> miniprep product</li>
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- | <li><b>Lane 6:</b> DNA ladder 1kb (biolabs)</li>
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- | <li><b>Lane 7:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB3C5) <b>1</b> miniprep product</li>
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- | <li><b>Lane 8:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB3C5) <b>2</b> miniprep product</li>
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- | <li><b>Lane 9:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>4</b> miniprep product</li>
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- | <li><b>Lane 10:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>3</b> miniprep product</li>
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- | <li><b>Lane 11:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>1</b> miniprep product</li>
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- | <li><b>Lane 12:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>2</b> miniprep product</li>
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- | <li><b>Lane 13:</b> DNA ladder 1kb (biolabs)</li></ul></div>
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- | <br/>
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- | <br/>
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- | We did some digestions (<a href="https://2012.igem.org/Team:Grenoble/Biology/Protocols/Restriction">protocol</a>) on GA miniprep (12/08/03). The digestions were achieved with XbaI during 10 minutes.<br/>
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- | <br/>
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- | To separate (<a href="https://2012.igem.org/Team:Grenoble/Biology/Protocols/Gel">protocol</a>) the digestion products, we prepared two 1.8% TAE agarose gels.<br/>
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- | Migration conditions = 100V during 30 min.<br/>
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- | In order to reveal the DNA fragments, we used <a href="https://2012.igem.org/Team:Grenoble/Biology/Protocols/EtBr">EtBr</a>.<br/>
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- | <br/>
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- | <center><img src="https://static.igem.org/mediawiki/2012/c/cd/120806_dig2.jpg" alt="photo_gel_28"/></center>
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- | <div class="legend"><p><center><u>Migration result for a 1.8% TAE agarose gel</u><br/>
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- | <i>(the DNA ladder scale is in kb)</i></center></p>
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- | <ul><li><b>Lane 1:</b> data not shown pAra/Bad_RBS_GFP_RBS_Cya (pSB3C5) <b>1</b> digestion product</li>
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- | <li><b>Lane 2:</b> data not shown pAra/Bad_RBS_GFP_RBS_Cya (pSB3C5) <b>1</b> miniprep product</li>
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- | <li><b>Lane 3:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB3C5) <b>2</b> digestion product</li>
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- | <li><b>Lane 4:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB3C5) <b>2</b> miniprep product</li>
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- | <li><b>Lane 5:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>4</b> digestion product</li>
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- | <li><b>Lane 6:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>4</b> miniprep product</li>
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- | <li><b>Lane 7:</b> DNA ladder 1kb (biolabs)</li>
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- | <li><b>Lane 8:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>3</b> digestion product</li>
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- | <li><b>Lane 9:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>3</b> miniprep product</li>
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- | <li><b>Lane 10:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>1</b> digestion product</li>
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- | <li><b>Lane 11:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>1</b> miniprep product</li>
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- | <li><b>Lane 12:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>2</b> digestion product</li>
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- | <li><b>Lane 13:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>2</b> miniprep product</li></ul></div>
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- | <br/>
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- | <br/>
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- | <br/>
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- | <center><img src="https://static.igem.org/mediawiki/2012/3/3e/120806.jpg" alt="photo_gel_29"/></center>
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- | <div class="legend"><p><center><u>Migration result for a 1.8% TAE agarose gel</u><br/>
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- | <i>(the DNA ladder scale is in kb)</i></center></p>
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- | <ul><li><b>Lane 1:</b> DNA ladder 1kb (biolabs)<br/>
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- | <li><b>Lane 2:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>4</b> digestion product</li>
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- | <li><b>Lane 3:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>4</b> miniprep product</li>
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- | <li><b>Lane 4:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>1</b> digestion product</li>
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- | <li><b>Lane 5:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>1</b> miniprep product</li>
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- | <li><b>Lane 6:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>2</b> digestion product</li>
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- | <li><b>Lane 7:</b> pAra/Bad_RBS_GFP_RBS_Cya (pSB4C5) <b>2</b> miniprep product</li>
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- | <li><b>Lane 8:</b> DNA ladder 80pb-10kb (fermentas)</li>
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- | </ul>
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- | </div>
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- | </section>
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- | <section>
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- | </div>
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- | </body>
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- | </html>
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- | {{:Team:Grenoble/script}}
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- | {{:Team:Grenoble/menu}}
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