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Team:TU-Delft/Protocol 3
From 2013.igem.org
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<li> <a href="https://2013.igem.org/Team:TU-Delft/Protocol_8" style="text-decoration: none""><font | <li> <a href="https://2013.igem.org/Team:TU-Delft/Protocol_8" style="text-decoration: none""><font | ||
color="#0080FF" size="3"> PCR Purification</font></a> </li> | color="#0080FF" size="3"> PCR Purification</font></a> </li> | ||
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| + | <li> <a href="https://2013.igem.org/Team:TU-Delft/Protocol_9" style="text-decoration: none""><font | ||
| + | color="#0080FF" size="3"> Tricine Gels</font></a> </li> | ||
</ul> | </ul> | ||
Revision as of 12:32, 29 September 2013
Protocols
Our project deals with E.coli cells which sense Auto-inducing peptides (AIPs) from the Staphylococcus aureus and starts producing Antimicrobial peptides in order to kill the Staphylococcus aureus. Different protocols used during the project are described below.
- Transforming Parts from Distribution kit
- Growing the Single Colonies from the Agar Plates
- Making glycerol stocks
- Miniprep Protocol
- Restriction digestion
- Ligation
- Gel Extraction Procedure
- PCR Purification
- Tricine Gels
Making glycerol stocks
Requirements:
- Glycerol
- Pipettes
- 1.5 mL Tubes
- Culture Sample
Prodecure:
- Label the tubes and add 180μL of glycerol.
- Pipette out 1000 μL of the culture.
- Add the culture to the tubes and store in -80°C
The glycerol stock can be used whenever required, by just adding 0.5 mL of stock into 5 mL of freshly prepared media.
