Team:Evry/Interlab Study/08-22-2014
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+ | <h2>Contructions PSB1C3 with I20260, J23101-E1010 and K823012-E1010</h2> | ||
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<br/> Transformation plate observation: | <br/> Transformation plate observation: | ||
- | <br/>- BBa_J23101: | + | <br/>- BBa_J23101: 11 isolated colonies |
- | <br/>- | + | <br/>- BBa_K823012: 100-150 isolated colonies |
<br/> | <br/> | ||
- | <br/> A PCR was performed | + | <br/> A PCR was performed with 8 colonies for BBa_K823012 and for BBa_J23101 following the protocol Table 3 and 4. |
<br/> To verify PCR products, 10 µl was loaded on a 1% agarose gel with 2 µl of loading dye 6X. | <br/> To verify PCR products, 10 µl was loaded on a 1% agarose gel with 2 µl of loading dye 6X. | ||
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- | <a href=" | + | <a href="https://static.igem.org/mediawiki/2014/2/28/22082014gel1-2_-_Copie.jpg" class="image"> |
- | <img alt="IMAGE" src=" | + | <img alt="IMAGE" src="https://static.igem.org/mediawiki/2014/2/28/22082014gel1-2_-_Copie.jpg" width="300px;" class="thumbimage"/> |
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- | <a href=" | + | <a href="https://static.igem.org/mediawiki/2014/2/28/22082014gel1-2_-_Copie.jpg" class="internal" title="Enlarge"> |
<img src="/wiki/skins/common/images/magnify-clip.png" width="15" height="11" alt="Symbol"/> | <img src="/wiki/skins/common/images/magnify-clip.png" width="15" height="11" alt="Symbol"/> | ||
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- | <center>1% agarose gel of PCR products | + | <center>1% agarose gel of PCR products. Lane 1 to 8: BBa_K823012 PCR products and Lane 9: Purple 2-Log. ladder NEB</center> |
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- | <br/> We expected to obtain a band between 300 and 400 bp. | + | <br/> We expected to obtain a band between 300 and 400 bp. So we decided to amplify the colony n°8. The colony was seed in 5 ml of LB medium and 5 µl of chloramphenicol. Culture was incubated overnight at 37°C with 200 rpm agitation. |
- | + | <div class="center"> | |
+ | <div class="thumb tnone"> | ||
+ | <div class="thumbinner" style="width:502px;"> | ||
+ | <a href="https://static.igem.org/mediawiki/2014/d/d5/Gel22082014bis.jpg" class="image"> | ||
+ | <img alt="IMAGE" src="https://static.igem.org/mediawiki/2014/d/d5/Gel22082014bis.jpg" width="500px;" class="thumbimage"/> | ||
+ | </a> | ||
+ | <div class="thumbcaption"> | ||
+ | <div class="magnify"> | ||
+ | <a href="https://static.igem.org/mediawiki/2014/d/d5/Gel22082014bis.jpg" class="internal" title="Enlarge"> | ||
+ | <img src="/wiki/skins/common/images/magnify-clip.png" width="15" height="11" alt="Symbol"/> | ||
+ | </a> | ||
+ | </div> | ||
+ | <center>1% agarose gel of PCR products. Lane 10 to 17: BBa_J23101 PCR products and Lane 9: Purple 2-Log ladder NEB</center> | ||
+ | </div> | ||
+ | </div> | ||
+ | </div> | ||
+ | </div> | ||
+ | <br/> | ||
+ | <br/> We expected to obtain a band around 1200 bp. So we decided to amplify the colony n°2 corresponding to lane 11. The colony was seed in 5 ml of LB medium and 5 µl of chloramphenicol. Culture was incubated overnight at 37°C with 200 rpm agitation. | ||
</p> | </p> |
Latest revision as of 17:59, 19 September 2014
Contructions PSB1C3 with I20260, J23101-E1010 and K823012-E1010
Transformation plate observation:
- BBa_J23101: 11 isolated colonies
- BBa_K823012: 100-150 isolated colonies
A PCR was performed with 8 colonies for BBa_K823012 and for BBa_J23101 following the protocol Table 3 and 4.
To verify PCR products, 10 µl was loaded on a 1% agarose gel with 2 µl of loading dye 6X.
We expected to obtain a band between 300 and 400 bp. So we decided to amplify the colony n°8. The colony was seed in 5 ml of LB medium and 5 µl of chloramphenicol. Culture was incubated overnight at 37°C with 200 rpm agitation.
We expected to obtain a band around 1200 bp. So we decided to amplify the colony n°2 corresponding to lane 11. The colony was seed in 5 ml of LB medium and 5 µl of chloramphenicol. Culture was incubated overnight at 37°C with 200 rpm agitation. Aug 22