Team:Paris-Saclay/Project/Notebook/Week 8
From 2012.igem.org
(Difference between revisions)
YohannPetiot (Talk | contribs) |
(→Week 8) |
||
(9 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 8'''= | |
- | [[Category:Team:Paris-Saclay/Project Gemote/Notebook| | + | |
+ | [[Category:Team:Paris-Saclay/Project Gemote/Notebook|h]] | ||
__NOTOC__ | __NOTOC__ | ||
====23rd July==== | ====23rd July==== | ||
Line 51: | Line 58: | ||
|- | |- | ||
| style="width: 50%;"|Electrophoresis of the post Gibson assembly PCR on a 1% Agarose gel. We are expecting a band at 4800bp for B, and a band at 1200bp for α and β. | | style="width: 50%;"|Electrophoresis of the post Gibson assembly PCR on a 1% Agarose gel. We are expecting a band at 4800bp for B, and a band at 1200bp for α and β. | ||
- | | style="width: 35%;"| [[File:Week8-1.jpg|right| | + | | style="width: 35%;"| [[File:Week8-1.jpg|right|400px]] |
|- | |- | ||
| style="width: 50%;"|Checking of the purity of BBa_K098995, BBa_K274100 and pSB1A2, all already digested by DPNI | | style="width: 50%;"|Checking of the purity of BBa_K098995, BBa_K274100 and pSB1A2, all already digested by DPNI | ||
Line 77: | Line 84: | ||
[[File:Week8-5.jpg|400px]] | [[File:Week8-5.jpg|400px]] | ||
+ | |||
PCR program used: | PCR program used: | ||
- | [[File:Week8-6.jpg| | + | |
+ | [[File:Week8-6.jpg|650px]] | ||
*Treatment by DPNI on BBa_K098995, BBa_K274100 and pSB1A2 in order to eliminate the plasmid matrix. | *Treatment by DPNI on BBa_K098995, BBa_K274100 and pSB1A2 in order to eliminate the plasmid matrix. | ||
Line 98: | Line 107: | ||
{{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 00:30, 27 September 2012
Week 8
23rd July
Electrophoresis of the post Gibson assembly PCR on a 1% Agarose gel. We are expecting a band at 4800bp for B, and a band at 1200bp for α and β. | |
Checking of the purity of BBa_K098995, BBa_K274100 and pSB1A2, all already digested by DPNI |
24th July
- Purification by column of BBa_K098995, BBa_K274100 and pSB1A2.
- Estimation of the concentration of BBa_K098995, BBa_K274100 and pSB1A2 by Nanovue.
Visualization of the purification of BBa_K098995, BBa_K274100 and pSB1A2 by electrophoresis on a 1% Agarose gel. We are expecting a band at 935 bp for BBa_K098995, 3385 pb for BBa_K274100 and 2079 bp for pSB1A2. |
25th July
- Amplification by PCR of BBa_K098995, BBa_K274100 and pSB1A2. Visualization by electrophoresis on a 1% Agarose gel. We are expecting a band at 935 bp for BBa_K098995, 3385 pb for BBa_K274100 and 2079 bp for pSB1A2.
PCR program used:
- Treatment by DPNI on BBa_K098995, BBa_K274100 and pSB1A2 in order to eliminate the plasmid matrix.
26th July
- Purification of BBa_K098995, BBa_K274100 and pSB1A2 with the gel extraction PCR clean up kit to prepare a Gibson assembly.
- Nanovue to measure the concentration of our 3 samples: BBa_K098995, BBa_K274100 and pSB1A2.
27th July
- Gibson assembly for the B construction (BBa_K115017 + 880bp end of BBa_K098995 + BBa_K274100 + BBa_J61048 + pSB1A2). A control is done with just the plasmid treated by DPNI.
- Transformation of competent cell DH5α with the B construction. Spreading out on LB+Agar+Ampicilline, and the Petri dishes are placed at 37°C.
Follow us !