GigiGoesGugu (Talk | contribs) (→Protocols) |
GigiGoesGugu (Talk | contribs) (→Protocols) |
||
| Line 12: | Line 12: | ||
[https://static.igem.org/mediawiki/2013/d/df/Team-EPF-Lausanne_Making_Nanoparticles.pdf Making Nanoparticles] <BR> | [https://static.igem.org/mediawiki/2013/d/df/Team-EPF-Lausanne_Making_Nanoparticles.pdf Making Nanoparticles] <BR> | ||
[https://static.igem.org/mediawiki/2013/6/6e/Team-EPF-Lausanne_Making_CompetentCell.pdf Making Competent Cells] <BR> | [https://static.igem.org/mediawiki/2013/6/6e/Team-EPF-Lausanne_Making_CompetentCell.pdf Making Competent Cells] <BR> | ||
| + | [https://static.igem.org/mediawiki/2013/d/de/Team-EPF-Lausanne_Gibson_Assembly.pdf] <BR> | ||
===Datasheets=== | ===Datasheets=== | ||
PCR
OD Measurements
PlateReader Measurements
Transforming Cells
Dialysis
ELISA-like Assay
Making Nanoparticles
Making Competent Cells
[1]
Below are listed the protocols we took directly from the datasheets/manufacturer instructions:
[http://www.piercenet.com/instructions/2160236.pdf Biotinylation]
[http://www.piercenet.com/instructions/2160383.pdf Chemically attaching streptavidin to bacterial surface] (using bacteria's outer glycoproteins)
"
