Team:UIUC-Illinois/Notebook/Protocols/Transformation
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- | <center><h1> | + | <center><h1>Electroporation and Transformation</h1></center><br/> |
+ | You will need:<br/><br/> | ||
+ | - 100 µl – Electrocompetent Cells<br/> | ||
+ | - 2-5 µl – Ligation Reaction (10 – 100 ng DNA)<br/> | ||
+ | - 1 ml – SOC broth/ LB liquid media<br/> | ||
+ | - Electrocuvette<br/><br/> | ||
+ | |||
+ | Procedure:<br/><br/> | ||
+ | 2. Gather all your supplies and keep them on ice (or in 4o C room). This includes the cuvettes. <br/> | ||
+ | 3. Thaw frozen electrocompetent cells on ice and place in electrocuvette. Then add ligation reaction and tap the cuvette to mix well. DO NOT pipette up and down.<br/> | ||
+ | 4. Keep on ice for 1 min.<br/> | ||
+ | 5. Pulse once (On machine use Ec1 for 1mm cuvettes and Ec2 for 2mm cuvettes).<br/> | ||
+ | 6. IMMEDIATELY after add 1ml of SOC broth and pipette up and down gently.<br/> | ||
+ | 7. Incubate recovering cells in 37o C for 1 hr.<br/><br/> | ||
+ | Plating:<br/><br/> | ||
+ | 1. After incubation, plate 200 µl of transformants on to appropriate selective plate and incubate at 37o C for 18+ hrs.<br/> | ||
+ | 2. If no colonies are formed plate out the rest of the transformants (~800 µl) and incubate at 37o C for 24 hrs<br/><br/> | ||
</div> | </div> | ||
Revision as of 15:27, 4 June 2012