McClean: Designing "Yeast Toolkit" compatible primers: Difference between revisions
New page: ==Overview== This protocol is written to prepare the user to design PCR primers such that the end product will have BsaI and BsmBI cut sites, as well as the correct flanking overhangs. It ... |
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Revision as of 15:57, 15 September 2016
Overview
This protocol is written to prepare the user to design PCR primers such that the end product will have BsaI and BsmBI cut sites, as well as the correct flanking overhangs. It is intended to supplement both 1. Lee, M. E., DeLoache, W. C., Cervantes, B. & Dueber, J. E. A Highly Characterized Yeast Toolkit for Modular, Multipart Assembly. ACS Synthetic Biology at <http://pubs.acs.org/doi/pdf/10.1021/sb500366v> (2015) and its own supplementary information.
Materials
- NCBI Primer-Blast (or other primer design tool)
- Basic understanding of Golden Gate Assembly (search for an overview in other websites if link doesn't work)
- An understanding of what DNA sequences BsaI and BsmBI recognize and where they cut.
Protocol
- Making Type 1 part
- 5'- GCATCGTCTCATCGGTCTCANNNN- gene of interest - NNNNTGAGACCTGAGACGGCAT -3'
- 3'- CGTAGCAGAGTAGCCAGAGTNNNN- gene of interest - NNNNACTCTGGACTCTGCCGTA -5'
- Step 2
- Step 3
Notes
Please feel free to post comments, questions, or improvements to this protocol. Happy to have your input!
- List troubleshooting tips here.
- You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
- Anecdotal observations that might be of use to others can also be posted here.
Please sign your name to your note by adding '''*~~~~''': to the beginning of your tip.
References
Gietz, R.D. and R.A. Woods. (2002) TRANSFORMATION OF YEAST BY THE Liac/SS CARRIER DNA/PEG METHOD. Methods in Enzymology 350: 87-96.
Contact
- Megan N McClean 14:01, 20 July 2011 (EDT)
or instead, discuss this protocol.
