Team:Groningen/Notebook/Wetwork 14August2012
From 2012.igem.org
(Difference between revisions)
Emeraldo88 (Talk | contribs) |
|||
(One intermediate revision not shown) | |||
Line 1: | Line 1: | ||
{{HeaderGroningen2012}} | {{HeaderGroningen2012}} | ||
- | < | + | <html> |
+ | <head> | ||
+ | <style type="text/css"> | ||
+ | p.margin | ||
+ | { | ||
+ | font-size:12pt; | ||
+ | line-height:14pt; | ||
+ | color:white; | ||
- | + | margin-top:0px; | |
+ | margin-bottom:20px; | ||
+ | margin-left:150px; | ||
+ | margin-right:250px; | ||
+ | } | ||
- | |||
- | + | </style> | |
+ | </head> | ||
- | Nisa | + | <body><br><br><br> |
- | + | <p class="margin"> | |
- | alsT promoter PCR -->OK! Proceeding to ligation and transformation tomorrow. | + | Tom<br> |
- | < | + | <br> |
+ | Ligation of Fnr promotor + GFP in psb1c3. Ratio of ligation 1:1:1 and 2:1:1 Fnr:GFP:psb1c3. <br> | ||
+ | <br> | ||
+ | Result: Transformation in E.coli did not work.<br> | ||
+ | <br> | ||
+ | Nisa<br> | ||
+ | <br> | ||
+ | alsT promoter PCR -->OK! Proceeding to ligation and transformation tomorrow.<br> | ||
+ | <br> | ||
+ | <br> | ||
+ | Emeraldo<br> | ||
+ | <br> | ||
+ | Another terminator+biobrick suffix and prefix PCR, cut the purified PCR product and pSac-Cm with EcoRI and HindIII, ligate both cut product and then transform E. coli with the ligated product. <br> | ||
+ | <br> | ||
<A HREF="https://2012.igem.org/Team:Groningen/Notebook"><FONT COLOR=#ff6700>Back to notebook</FONT></A> | <A HREF="https://2012.igem.org/Team:Groningen/Notebook"><FONT COLOR=#ff6700>Back to notebook</FONT></A> | ||
+ | <br><br></p></body> | ||
</html> | </html> | ||
{{Template:SponsorsGroningen2012}} | {{Template:SponsorsGroningen2012}} |
Latest revision as of 13:31, 26 September 2012
Tom
Ligation of Fnr promotor + GFP in psb1c3. Ratio of ligation 1:1:1 and 2:1:1 Fnr:GFP:psb1c3.
Result: Transformation in E.coli did not work.
Nisa
alsT promoter PCR -->OK! Proceeding to ligation and transformation tomorrow.
Emeraldo
Another terminator+biobrick suffix and prefix PCR, cut the purified PCR product and pSac-Cm with EcoRI and HindIII, ligate both cut product and then transform E. coli with the ligated product.
Back to notebook