Team:Paris-Saclay/Project/Notebook/Week 10
From 2012.igem.org
(Difference between revisions)
YohannPetiot (Talk | contribs) |
(→7th August) |
||
(4 intermediate revisions not shown) | |||
Line 23: | Line 23: | ||
</head> | </head> | ||
<body> | <body> | ||
- | <div id="single- | + | <div id="tiles"> |
- | <div | + | <div id="single-tile3" class="red live-tile" data-mode="flip" data-delay="4000"> |
- | + | <div> | |
- | + | <a href="https://2012.igem.org/Team:Paris-Saclay/Project/Abstract"> | |
- | + | <div class="child-tile"><p class="child-tile">GEMOTE Project</p></div> | |
+ | <img src="https://static.igem.org/mediawiki/2012/7/7c/Project-1.png" alt="" /> | ||
+ | </a> | ||
+ | </div> | ||
<div> | <div> | ||
- | <img src=" | + | <a href="https://2012.igem.org/Team:Paris-Saclay/Project/Abstract"> |
- | + | <img src="https://static.igem.org/mediawiki/2012/d/d1/Project2.jpg" alt="" /> | |
+ | <div class="child-tile"><p class="child-tile">GEMOTE Project</p></div> | ||
+ | </a> | ||
</div> | </div> | ||
- | <script type="text/javascript"> | + | </div> |
+ | <script type="text/javascript"> | ||
// apply regular slide universally unless .exclude class is applied | // apply regular slide universally unless .exclude class is applied | ||
// NOTE: The default options for each liveTile are being pulled from the 'data-' attributes | // NOTE: The default options for each liveTile are being pulled from the 'data-' attributes | ||
$(".live-tile, .flip-list").not(".exclude").liveTile(); | $(".live-tile, .flip-list").not(".exclude").liveTile(); | ||
- | </script> | + | </script> |
- | </div> | + | </div> |
</body> | </body> | ||
</html> | </html> | ||
Line 43: | Line 49: | ||
</div> | </div> | ||
<div id="content-paris-saclay"> | <div id="content-paris-saclay"> | ||
- | + | ='''Week 10'''= | |
+ | |||
[[Category:Team:Paris-Saclay/Project Gemote/Notebook|j]] | [[Category:Team:Paris-Saclay/Project Gemote/Notebook|j]] | ||
__NOTOC__ | __NOTOC__ | ||
Line 56: | Line 63: | ||
*Liquid culture of B1 in order to prepare a glycerol stock | *Liquid culture of B1 in order to prepare a glycerol stock | ||
- | ** | + | **Reception of new primers |
**2 Forward | **2 Forward | ||
**3 Reverse | **3 Reverse | ||
**Plasmid Reverse | **Plasmid Reverse | ||
- | |||
====8th August==== | ====8th August==== | ||
Line 115: | Line 121: | ||
{{Team:Paris-Saclay/Follow}} | {{Team:Paris-Saclay/Follow}} | ||
+ | </div> | ||
</div> | </div> | ||
</div> | </div> | ||
{{Team:Paris-Saclay/Footer}} | {{Team:Paris-Saclay/Footer}} |
Latest revision as of 00:32, 27 September 2012
Week 10
6th August
- Sending of the B1 sample to sequencing with two pairs of primers
- K-274100 Forward and Reverse
- Plasmid pSB1A2 Forward and Reverse
7th August
- Liquid culture of B1 in order to prepare a glycerol stock
- Reception of new primers
- 2 Forward
- 3 Reverse
- Plasmid Reverse
8th August
Amplification of the plasmid pSB1A2, BBa_K274100 and BBa_K115017 by PCR with the new primers. Visualization by electrophoresis on a 2% Agarose gel for BBa_K115017 and a 0.8% Agarose gel for BBa_K274100 and the plasmid pSB1A2. We are expecting a band at 147 bp for BBa_K115017, 3408 bp for BBa_K274100 and 2079 for the plasmid. |
9th August
New amplification by PCR of the plasmid pSB1A2, BBa_K274100 and BBa_K115017 as it has been done the day before. |
- Digestion by EcoRI of the plasmid that contains BBa_K274100.
10th August
Amplification by PCR of BBa_K274100 already digested by EcoRI. Visualization by electrophoresis on a 0.8% Agarose gel. |
Miniprep of BBa_K274100 followed by Nanovue to determine the concentration of the sample | |
Miniprep of the Plasmid pSB1A2 followed by Nanovue to determine the concentration of the sample |
- Digestion by HindIII of the plasmid pSB1A2 in order to linearize it.
Digestion of BBa_K115017 by DPNI to eliminate the plasmid matrix. Visualization by electrophoresis on a 2% Agarose gel. We are expecting a band at 123 bp. |
Follow us !