Team:Paris/August 13
From 2008.igem.org
(Difference between revisions)
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*10 µL loaded | *10 µL loaded | ||
- | {|border="1" | + | {| style="text-align: center;" border="1" |
- | + | |'''well n°''' | |
- | + | |1 | |
- | + | |2 | |
- | + | |3 | |
- | + | |4 | |
- | + | |5 | |
- | + | |6 | |
- | + | |7 | |
- | + | |8 | |
|- | |- | ||
- | + | |'''sample''' | |
- | + | |100 bp DNA ladder | |
- | + | |positive control | |
- | + | |negative control | |
- | + | |'''L130.3''' | |
- | + | |'''L130.4''' | |
- | + | |'''L130.5''' | |
- | + | |'''L130.6''' | |
- | + | |PCR product (L130.8) purified by the Qiaquick Gel Extraction kit | |
|- | |- | ||
- | + | |'''red fluorescence''' | |
|rowspan="3"| | |rowspan="3"| | ||
- | + | |strain a little bit pink | |
- | + | |not concerned | |
- | + | |no | |
- | + | |no | |
- | + | |no | |
- | + | |no | |
- | |rowspan="3"| | + | |rowspan="3"|not concerned / doesn't matter</center> |
|- | |- | ||
- | + | |'''expected size''' | |
- | + | |1,161 kb | |
- | + | |0 kb | |
|colspan="4"|<center>'''1,338 kb'''</center> | |colspan="4"|<center>'''1,338 kb'''</center> | ||
|- | |- | ||
- | + | |'''measured size''' | |
- | | | + | |style="background: #cbff7B"| 1,2 kb |
- | | | + | |style="background: #cbff7B"| 0 kb |
- | | | + | |style="background: #cbff7B"| 1,2 kb |
- | | | + | |style="background: #cbff7B"| 1,2 kb |
- | | | + | |style="background: #cbff7B"| 1,2 kb |
- | | | + | |style="background: #cbff7B"| 1,2 kb |
|} | |} | ||
Revision as of 16:00, 15 August 2008
Sequencing Minipreps we did yesterday
Minipreps: Plasmid extraction
Glycerol Stocks
Assay to purify a PCR product using the Qiaquick Gel Extraction kit
=> see Gel 1, well n° 8 ==> results: PCR products can be purified using the Qiaquick Gel Extraction kit. We just have to replace the buffer PBI by the buffer QG! PCR screening4 more transformants of L130 (pFlhB into J61002) are screened by PCR.
Electrophoresis
==> The L130 transformants analysed are not correct. Transformation of the ligation we did yesterdayWe transformed L 139, L140, L141 and L142 following the standard protocol using Invitrogen's TOP 10 chemically competent cells. The positive control is a transformation with pUC19 and the negative control has no plasmid. Promoter Characterization: work plan |