Team:Paris/August 19
From 2008.igem.org
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{{Paris/Calendar_Links|August 18|August 20}} | {{Paris/Calendar_Links|August 18|August 20}} | ||
+ | =Screening of the cloning of OmpR*, EnvZ* and FlhDC+promotor= | ||
- | ==Ligation FC | + | {|border="1" style="text-align: center" |
+ | |'''well n°''' | ||
+ | |1 | ||
+ | |2 | ||
+ | |3 | ||
+ | |4 | ||
+ | |5 | ||
+ | |6 | ||
+ | |7 | ||
+ | |8 | ||
+ | |9 | ||
+ | |10 | ||
+ | |11 | ||
+ | |12 | ||
+ | |13 | ||
+ | |- | ||
+ | |'''sample''' | ||
+ | |1 kb DNA ladder | ||
+ | |positive control: pSB3K3 (strain S158) | ||
+ | |negative control: no template | ||
+ | |L133.1 | ||
+ | |L133.2 | ||
+ | |L133.3 | ||
+ | |L134.1 | ||
+ | |L134.2 | ||
+ | |L134.3 | ||
+ | |L132.1 | ||
+ | |L132.2 | ||
+ | |L132.3 | ||
+ | |1 kb DNA ladder | ||
+ | |- | ||
+ | |'''expected size''' | ||
+ | | | ||
+ | |about 1 kb | ||
+ | |0 kb | ||
+ | |colspan="3"| | ||
+ | |colspan="3"| | ||
+ | |colspan="3"| | ||
+ | | | ||
+ | |- | ||
+ | |'''measured size''' | ||
+ | | | ||
+ | |1 kb | ||
+ | |0 kb | ||
+ | | | ||
+ | |0 kb | ||
+ | |0 kb | ||
+ | |0 kb | ||
+ | | | ||
+ | | | ||
+ | | | ||
+ | | | ||
+ | | | ||
+ | | | ||
+ | |} | ||
+ | |||
+ | |||
+ | =Ligation FC= | ||
=Screening of the cloning of E0240 and FlhDC+promotor= | =Screening of the cloning of E0240 and FlhDC+promotor= |
Revision as of 15:22, 19 August 2008
Screening of the cloning of OmpR*, EnvZ* and FlhDC+promotor
Ligation FCScreening of the cloning of E0240 and FlhDC+promotorSpreading the clones in order to obtain single colonies
The PCR screening of the transformants L139 and L142 of august 15th revealed several bands for a given clone including one band appearing at the right size.
In order to check these 2 hypothesis and to isolate (if it is possible) the right clone (containing the plasmid with the insert). We decided to spread the "clone" in question in a LB plate in order to carry out a PCR screening on single colonies.
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