"
Team:Paris/Protocols
From 2009.igem.org
(Difference between revisions)
Christophe.R (Talk | contribs) (→1. Microscopy) |
Christophe.R (Talk | contribs) (→1. Microscopy) |
||
| Line 17: | Line 17: | ||
==Summary== | ==Summary== | ||
===1. Microscopy=== | ===1. Microscopy=== | ||
| - | * [[Team:Paris/ | + | * [[Team:Paris/ProtocolsA#Protocols suggested | Protocols suggested]] |
===2. Adapted Protocols=== | ===2. Adapted Protocols=== | ||
Revision as of 20:59, 9 August 2009
Contents |
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.
Summary
1. Microscopy
2. Adapted Protocols
- DNA extraction
- Mini prep
- Gel/PCR Purification
3. Culture protocols
- Over Night
- Transformation
- Competent bacterias
- Glycerol stock
4. Molecular biology
- PCR
- Gels
- Digestion
- Ligation
- Protocol to make competent bacteria
- Protocole PCR quick load Taq mix
- [http://probes.invitrogen.com/media/pis/mp00282.pdf Protocol to membrane dying, DID method]
- Adaptation of PureYield™ Plasmid Miniprep System
- Protocol for bacterial transformation
A.2. iGEM paris 2008 protocols link
content :
- Electrophoresis
- Concentration of the Miniprep or the Midiprep
- Amplification of promoters.
- PCR Screening
- Protocol to make competent bacteria
A.3. 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
