Team:CSU Fort Collins/Notebook/Protocols=Purify
From 2014.igem.org
(Difference between revisions)
Line 794: | Line 794: | ||
<br><br> | <br><br> | ||
- | <center><a href='/Team:CSU_Fort_Collins/Notebook/Protocols= | + | <center><a href='/Team:CSU_Fort_Collins/Notebook/Protocols=Gel' id='navi' style='margin-left:-20px; margin-right:40px'> Previous</a> |
</div> | </div> | ||
Revision as of 16:45, 17 October 2014
PCR Product Purification Protocol
Show Table of Contents
-
- Adjust total volume of all PCR tubes to 100 μL
- Add 500 μL Binding Buffer to each tube
- Mix well
-
- Insert one High Pure filter tube into one collection tube
- Transfer solution from 1 into the filter
- Centrifuge 60 seconds at maximum speed
-
- Disconnect filter tube and discard flow-through
- Reconnect tubes
-
- Add 500 μL wash buffer to upper reservoir
- Centrifuge 60 seconds at maximum speed
-
- Discard the flow-through
- Recombine tubes
- Add 200 μL wash buffer
- Centrifuge for 60 seconds at maximum speed
-
- Discard flow-through and collection tube
- Reconnect filter tube to a clean 1.5 mL centrifuge tube
-
- Add 100 μL elution buffer
- Centrifuge for 1 minute at maximum speed
-
- The purified PCR product is now in the microcentrifuge tube
- Store at 4 °C for short term or at -20 °C for later use