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{{Template:EPFL2013Header}} | {{Template:EPFL2013Header}} | ||
<font size = "4"> Cell Surface Display </font> | <font size = "4"> Cell Surface Display </font> | ||
| - | |||
| - | '' | + | ''MiniPrep''<BR> |
| + | We did a Miniprep of Streptavidin iGEM cells that were inoculated the day before. | ||
| + | <BR><BR> | ||
| - | < | + | <font size = "4"> Nanoparticles </font> |
| - | <br>- Learned how to use the DLS. Measured the DGPs+dye. Results: not good, the machine could not measure anything because the digested GPs were aggregated. | + | |
| + | ''Making Nanoparicles, 1st try'' <BR> | ||
| + | - Vacuum drying and purification of the digested GPs+dye. | ||
| + | <br>- Learned how to use the DLS. Measured the DGPs+dye. <BR> Results: not good, the machine could not measure anything because the digested GPs were aggregated and too concentrated. | ||
<br>- Vacuum drying and purification of the new GPs. | <br>- Vacuum drying and purification of the new GPs. | ||
{{Template:EPFL2013Footer}} | {{Template:EPFL2013Footer}} | ||
MiniPrep
We did a Miniprep of Streptavidin iGEM cells that were inoculated the day before.
Nanoparticles
Making Nanoparicles, 1st try
- Vacuum drying and purification of the digested GPs+dye.
- Learned how to use the DLS. Measured the DGPs+dye.
Results: not good, the machine could not measure anything because the digested GPs were aggregated and too concentrated.
- Vacuum drying and purification of the new GPs.
"
