"
Team:EPF-Lausanne/Notebook/September2011
From 2011.igem.org
(Difference between revisions)
(→Thursday, September 1 2011) |
|||
| Line 4: | Line 4: | ||
== Thursday, September 1 2011 == | == Thursday, September 1 2011 == | ||
| + | |||
| + | After taking a closer look at the plate from the platereader, it seems that none of the T7 variants did any lysing. This realization made it urgent that we discover whether or not the full T4-lysis cassette was really in these Gibson-assembled plasmids. The samples that had been sent in for sequencing had primers that seemed to amplify the backbone, instead of the lysis cassette. While this does not necessarily mean that the lysis is not there, it does suggest that all the PCRS and gels used to verify the presence of lysis were only showing the existence of the backbone. | ||
| + | |||
| + | Alina ran a PCR with different primers from Douglas' first attempts at putting together the 2700 bp cassette that amplify select regions of the cassette. | ||
{{:Team:EPF-Lausanne/Templates/Footer|title=Notebook: September 2011}} | {{:Team:EPF-Lausanne/Templates/Footer|title=Notebook: September 2011}} | ||
Revision as of 07:57, 2 September 2011
Notebook: September 2011
Thursday, September 1 2011
After taking a closer look at the plate from the platereader, it seems that none of the T7 variants did any lysing. This realization made it urgent that we discover whether or not the full T4-lysis cassette was really in these Gibson-assembled plasmids. The samples that had been sent in for sequencing had primers that seemed to amplify the backbone, instead of the lysis cassette. While this does not necessarily mean that the lysis is not there, it does suggest that all the PCRS and gels used to verify the presence of lysis were only showing the existence of the backbone.
Alina ran a PCR with different primers from Douglas' first attempts at putting together the 2700 bp cassette that amplify select regions of the cassette.
