"
Team:University of Ottawa/26 June 2008
From 2008.igem.org
(Difference between revisions)
Djedrysiak (Talk | contribs)
(New page: __TOC__ '''Dan''' :'''PCR gel''' ::<li>The gel turned out well, S&D&T amplification products had some non specific binding, but there was enough separation to cut the good bands out and pu...)
Newer edit →
(New page: __TOC__ '''Dan''' :'''PCR gel''' ::<li>The gel turned out well, S&D&T amplification products had some non specific binding, but there was enough separation to cut the good bands out and pu...)
Newer edit →
Revision as of 18:04, 30 June 2008
Dan
- PCR gel
- The gel turned out well, S&D&T amplification products had some non specific binding, but there was enough separation to cut the good bands out and purify.
- After PCR cleanup (for 0&1 amplification products) and gel extraction and cleanup (for S&D&T plasmids) absorbtion was measured in order to determine the concentration of the PCR products.
- S&D&T amplification products showed low DNA concentration, however it is still
