Imperial College/15 October 2008
From 2008.igem.org
(Difference between revisions)
m |
|||
(5 intermediate revisions not shown) | |||
Line 7: | Line 7: | ||
| rowspan="2" bgcolor=#ffffff width="100%" | | | rowspan="2" bgcolor=#ffffff width="100%" | | ||
|} | |} | ||
- | + | =15 October 2008= | |
===Wet Lab=== | ===Wet Lab=== | ||
- | + | ||
- | *Today | + | ===Digestion of minipreps=== |
+ | |||
+ | *Today minipreps were prepared. These were digested and run on a gel to confirm the presence of the correct constructs. The folowing constructs were minipreped: Gene art 14 (pXyl-spoVG) and 5' EpsE integration sites. | ||
+ | |||
+ | *To test that insert with the correct size is present in the plasmid, the minipreps were digestd with EcoRI and PstI. The image below shows the results: | ||
[[Image:Wednesday15thoct.PNG|center|400px]] | [[Image:Wednesday15thoct.PNG|center|400px]] | ||
- | *Several of construct 14 | + | *Several of construct 14 appear to have succssfully been ligated. In addition all of the 5'EpsE appear to have worked. |
+ | <br> | ||
+ | {{Imperial/EndPage|Notebook|Notebook}} | ||
+ | |||
+ | *To construct 5'EpsE integration site we used a PCR product and as a result of the approach, there is a possibility that the orientation of this biobrick in the vector is incorrect. Digestion with XbaI SpeI will confirm correct orientation. | ||
+ | |||
+ | |||
+ | [[Image:Wednesday15thoct2.PNG|center|400px]] | ||
- | * | + | *If the PCR product has the correct orientation then the insert will fall out with this digestion. Clearly only 5'EpsE-1 is correct. |
Latest revision as of 20:51, 28 October 2008
15 October 2008Wet LabDigestion of minipreps
|