Imperial College/15 October 2008
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===Wet Lab=== | ===Wet Lab=== | ||
+ | ====Digestion of mini's==== | ||
*Today mini preps were prepared. These were digested and run on a gel to confirm the presence of the correct constructs. The folowing constructs were mini preped; Gene art 14 (pXyl-spoVG) and 5' EpsE integration sites. To test the correct size insert is present the mini's were digestd with EcoRI and PstI. The image below shows the results: | *Today mini preps were prepared. These were digested and run on a gel to confirm the presence of the correct constructs. The folowing constructs were mini preped; Gene art 14 (pXyl-spoVG) and 5' EpsE integration sites. To test the correct size insert is present the mini's were digestd with EcoRI and PstI. The image below shows the results: | ||
[[Image:Wednesday15thoct.PNG|center|400px]] | [[Image:Wednesday15thoct.PNG|center|400px]] | ||
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+ | *Several of construct 14 have appeared to have succssfully been ligated. In addition all of the 5'EpsE appear to have worked. | ||
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+ | *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. |
Revision as of 14:17, 19 October 2008
Wet LabDigestion of mini's
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