"
Team:Uppsala-SwedenWeek12
From 2010.igem.org
(→Construction of H1- G8) |
(→Construction of H1- G8) |
||
| Line 19: | Line 19: | ||
The samples selected in Colony PCR were inoculated for obtaining material to do plasmid extraction. Overnight culture was used to make glycerol stocks and plasmids were extracted. The plasmid concentration was measured for estimating the amount of enzymes required for digestion and ligation. | The samples selected in Colony PCR were inoculated for obtaining material to do plasmid extraction. Overnight culture was used to make glycerol stocks and plasmids were extracted. The plasmid concentration was measured for estimating the amount of enzymes required for digestion and ligation. | ||
| + | |||
| + | Plasmids were digested with proper enzymes bought from Sigma-Aldrich and run for gel to confirm the size. The plasmid parts where also digested for use in ligation for the next step.The correct set of parts was ligated using Ampicillin backbone via 3A assembly following the Flowchart as per the plan. | ||
Revision as of 18:08, 26 October 2010
Week-12
Construction of H1- G8
5 colonies were picked from each of those plates and sent to perform c-PCR. According to the band size on gel picture, 1 or 2 colonies of each set were selected to inoculate.
From the above gel picture it was not very clear. Some fiddling around with the controls and we got a much better image (given below).
.jpg)
.jpg)
.jpg)
The samples selected in Colony PCR were inoculated for obtaining material to do plasmid extraction. Overnight culture was used to make glycerol stocks and plasmids were extracted. The plasmid concentration was measured for estimating the amount of enzymes required for digestion and ligation.
Plasmids were digested with proper enzymes bought from Sigma-Aldrich and run for gel to confirm the size. The plasmid parts where also digested for use in ligation for the next step.The correct set of parts was ligated using Ampicillin backbone via 3A assembly following the Flowchart as per the plan.
