Team:TUDelft/9 September 2009
From 2009.igem.org
(Difference between revisions)
Tim Weenink (Talk | contribs) (New page: {{Template:TUDelftiGEM2009}} {{Template:TUDelftiGEM2009_LabNotebook}} ='''9 September 2009'''= {{Template:TUDelftiGEM2009_end}}) |
(→9 September 2009) |
||
Line 4: | Line 4: | ||
='''9 September 2009'''= | ='''9 September 2009'''= | ||
+ | ===Sriram=== | ||
+ | Today I did the miniprep of the cultures inoculated yesterday. Also did a restriction to analyse the sizes of the products. It can be seen in the gel image below. | ||
+ | [[Image:Sriram-Delay090909new1.jpg|thumb|center|450px]] | ||
+ | From the gel it is clear that we have all the assemblies of proper sizes. The only troubling thing was the positive control GFP glowing colony gave a correct band while the non-GFP glowing colony is not of proper size. It is possible due to different assemblies that could be got from electroporation of ligated products. | ||
{{Template:TUDelftiGEM2009_end}} | {{Template:TUDelftiGEM2009_end}} |
Latest revision as of 23:29, 21 October 2009
Lab Notebook
|
|
|
|
9 September 2009
Sriram
Today I did the miniprep of the cultures inoculated yesterday. Also did a restriction to analyse the sizes of the products. It can be seen in the gel image below.
From the gel it is clear that we have all the assemblies of proper sizes. The only troubling thing was the positive control GFP glowing colony gave a correct band while the non-GFP glowing colony is not of proper size. It is possible due to different assemblies that could be got from electroporation of ligated products.