"
Team:Paris/Protocols
From 2009.igem.org
(Difference between revisions)
(→Protocols) |
(→Protocols) |
||
| Line 18: | Line 18: | ||
[[Team:Paris/Protocols_Competent_Bacteria | Protocol to make competent bacteria]] | [[Team:Paris/Protocols_Competent_Bacteria | Protocol to make competent bacteria]] | ||
| + | [[Team:Paris/Protocols_PCRqload | Protocole PCR quick load Taq mix]] | ||
| + | |||
---- | ---- | ||
Revision as of 08:08, 28 July 2009
Protocols
Here you will find the collection of protocole we use, or just collect. And because we are well-known chauvinist it is just a tribute to previous Paris iGEM team . We try our best not to make it redondant.
iGEM paris 2009 protocols link :
our protocol:
Protocol to make competent bacteria Protocole PCR quick load Taq mix
iGEM paris 2008 protocols link :
content :
- Electrophoresis
- Concentration of the Miniprep or the Midiprep
- Amplification of promoters.
- PCR Screening
- Protocol to make competent bacteria
iGEM paris 2007 protocols link :
[http://parts.mit.edu/igem07/index.php/Paris/PROTOCOLS Click here]
content :
- Growing_bacteria_in_liquid_medium
- Preparing growth media
- exemple: Making 10 petri dish (LB+erythromycin+citrate+DAP), Solid M9 Minimum Medium, preparation of agarosis gel
- Chemical transformation
- Glycerol Stock
- Recombineering/Lambda red-mediated gene replacement
- Miniprep
- Fluorescent single cells visualisation
- Digestion reactions
Protocols suggested
still waiting for it...
