BUGSS:Build-a-BUG:2-2: Difference between revisions
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* [http://openwetware.org/images/f/fe/QIAquick-Gel-Extraction-Kit-EN.pdf QIAquick Gel Extraction Protocol] and [http://openwetware.org/images/7/7f/EN-QIAquick-Spin-Handbook.pdf Handbook] | * [http://openwetware.org/images/f/fe/QIAquick-Gel-Extraction-Kit-EN.pdf QIAquick Gel Extraction Protocol] and [http://openwetware.org/images/7/7f/EN-QIAquick-Spin-Handbook.pdf Handbook] | ||
=== Restriction endonucleases === | === Restriction endonucleases and DNA ladder === | ||
* [https://www.neb.com/products/r0101-ecori EcoRI] | * [https://www.neb.com/products/r0101-ecori EcoRI] | ||
* [https://www.neb.com/products/r0145-xbai XbaI] | * [https://www.neb.com/products/r0145-xbai XbaI] | ||
* [https://www.neb.com/products/r0133-spei SpeI] | * [https://www.neb.com/products/r0133-spei SpeI] | ||
* [https://www.neb.com/products/r0140-psti PstI] | * [https://www.neb.com/products/r0140-psti PstI] | ||
* [https://www.neb.com/products/N3232-1-kb-DNA-Ladder 1 kb DNA Ladder] | |||
== Notes == | |||
* We ran samples of our BBa_K801000 (pTUM100) and BBa_K165057 (Kozak + mCherry) plasmid DNA minipreps from Session 1 on an agarose gel with a 1 kb DNA ladder (to measure size). We also ran some BBa_K165057 (Kozak + mCherry) plasmid DNA that had been digested with XbaI and SpeI enzymes. | |||
* We did restriction digests on our BBa_K801000 (pTUM100) plasmid DNA minipreps from Session 1 using EcoRI and PstI enzymes. | |||
* We excised the BBa_K165057 (Kozak + mCherry) DNA fragment from our agarose gels. Then we recovered the DNA using the QIAquick Gel Extraction kit. | |||
* We cleaned up our digested BBa_K801000 (pTUM100) vectors using columns and reagents from the QIAquick Gel Extraction kit. | |||
</div> | </div> | ||
Revision as of 22:18, 3 March 2013
Home Contact Internal Lab Members Projects Protocols Build-a-BUG Build-a-Gene 2016 Build-a-Gene 2015 Build-a-Gene 2014 Build-a-Gene 2013 Chalk Talks
Build-a-BUG: Series 2, Session 2
Saturday, February 23, 2013
Noon to 4:00 PM
This is the second Build-A-BUG workshop in a series of five on yeast. You will continue to hone your basic lab techniques, including pipetting and centrifugation, while continuing either your own or somebody else's mating type detector project. This lab will involve restriction digests (cutting DNA), agarose gel electrophoresis (visualizing DNA), gel extractions (recovering DNA fragments), and column-based DNA purifications.
Background reading
Protocols
- Optimizing Restriction Endonuclease Reactions
- Agarose gel electrophoresis
- QIAquick Gel Extraction Protocol and Handbook
Restriction endonucleases and DNA ladder
Notes
- We ran samples of our BBa_K801000 (pTUM100) and BBa_K165057 (Kozak + mCherry) plasmid DNA minipreps from Session 1 on an agarose gel with a 1 kb DNA ladder (to measure size). We also ran some BBa_K165057 (Kozak + mCherry) plasmid DNA that had been digested with XbaI and SpeI enzymes.
- We did restriction digests on our BBa_K801000 (pTUM100) plasmid DNA minipreps from Session 1 using EcoRI and PstI enzymes.
- We excised the BBa_K165057 (Kozak + mCherry) DNA fragment from our agarose gels. Then we recovered the DNA using the QIAquick Gel Extraction kit.
- We cleaned up our digested BBa_K801000 (pTUM100) vectors using columns and reagents from the QIAquick Gel Extraction kit.
