Team:Macquarie Australia/WetLab/Protocols/PlasmidPreps
From 2014.igem.org
(Difference between revisions)
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<div class="cont-out"> | <div class="cont-out"> | ||
- | <h3>Plasmid Prep</h3> | + | <h3>Plasmid Prep</h3><br/> |
- | < | + | |
+ | <ul style="list-style-type: decimal;"> | ||
+ | <li>Centrifuge @13,200 rpm for 10 min of 1.8mL of overnight cultures in 2mL Eppendorf’s</li> | ||
+ | <li>Discard supernatant and add 1.9 mL of culture and centrifuge again @13,200 rpm for 10 min</li> | ||
+ | <li>Re-suspend pelleted cells in P1 Buffer (250µl) </li> | ||
+ | <li>Add 250µL of P2 buffer & invert 4-6 times (turns homogenous blue)</li> | ||
+ | <li>Add 350µL of N3 & mix by inverting (turns colourless)</li> | ||
+ | <li>Centrifuge @ 10min 13,000 rpm to obtain a pellet</li> | ||
+ | <li>Transfer supernatant in QIA Prep Spin Column by pipetting</li> | ||
+ | <li>Centrifuge 30-60 sec - discard flow through</li> | ||
+ | <li>Wash QIA Prep Spin Column with 0.5mL of PB</li> | ||
+ | <li>Centrifuge for 30-60 seconds - discard flow through</li> | ||
+ | <li>Wash spin column by adding 0.75 mL PE buffer</li> | ||
+ | <li>Centrifuge for 30-60 seconds - discard flow through and centrifuge for a further 1min</li> | ||
+ | <li>Place QIAPrep Column in clean Eppendorf</li> | ||
+ | <li>Elute DNA add 50µl of water, stand for 1min, centrifuge for 1min</li> | ||
+ | <li>QIA prep - Spin miniprep buffer</li> | ||
+ | </ul> | ||
+ | |||
</div> | </div> | ||
</section> | </section> | ||
</body> | </body> | ||
</html> | </html> |
Revision as of 05:09, 16 October 2014
Plasmid Prep
- Centrifuge @13,200 rpm for 10 min of 1.8mL of overnight cultures in 2mL Eppendorf’s
- Discard supernatant and add 1.9 mL of culture and centrifuge again @13,200 rpm for 10 min
- Re-suspend pelleted cells in P1 Buffer (250µl)
- Add 250µL of P2 buffer & invert 4-6 times (turns homogenous blue)
- Add 350µL of N3 & mix by inverting (turns colourless)
- Centrifuge @ 10min 13,000 rpm to obtain a pellet
- Transfer supernatant in QIA Prep Spin Column by pipetting
- Centrifuge 30-60 sec - discard flow through
- Wash QIA Prep Spin Column with 0.5mL of PB
- Centrifuge for 30-60 seconds - discard flow through
- Wash spin column by adding 0.75 mL PE buffer
- Centrifuge for 30-60 seconds - discard flow through and centrifuge for a further 1min
- Place QIAPrep Column in clean Eppendorf
- Elute DNA add 50µl of water, stand for 1min, centrifuge for 1min
- QIA prep - Spin miniprep buffer