Difference between revisions of "Part:BBa K165046"
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GAL2ko.rev: AATACTCTGATATATGTACACAAATAATAGGTTTAGGTAAGGAATTTATATAATCGTAAG '''TTCGAGCTCGTTTAAAC''' | GAL2ko.rev: AATACTCTGATATATGTACACAAATAATAGGTTTAGGTAAGGAATTTATATAATCGTAAG '''TTCGAGCTCGTTTAAAC''' | ||
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+ | Transform the product into yeast by standard procedure [http://www.natureprotocols.com/2007/01/31/highefficiency_yeast_transform.php], and select transformants with G418 YPD plates | ||
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Revision as of 03:57, 31 October 2008
pGAL1+ Kozak
The pGAL promoter is induced by the presence of galactose and repressed by glucose. Raffinose is used as a neutral carbon source, with no effect on pGAL1. The promoter normally has an all-or-nothing response. To make it tunable, knock out the Gal2 gene.[http://www.jbc.org/cgi/content/abstract/M512317200v1]
Use these primers on a Kan resistance gene template: (the portion in bold binds to the template, the rest is homologous to the Gal2 gene on the yeast chromosome.)
GAL2ko.fwd: AGCAGCAAAA CATTAATTTT GCTTCCAAGA CGACAGTAAT ATGTCTCCTA CAATACCAGT GGCAGATCCGCTAGGGATAA
GAL2ko.rev: AATACTCTGATATATGTACACAAATAATAGGTTTAGGTAAGGAATTTATATAATCGTAAG TTCGAGCTCGTTTAAAC
Transform the product into yeast by standard procedure [http://www.natureprotocols.com/2007/01/31/highefficiency_yeast_transform.php], and select transformants with G418 YPD plates
To check for proper knockout, amplify the section of the chromosome where the insert should be. Use these primers:
GAL2kosc.fwd: TGTGCATGTT ATCTATATCC TTCTTTATAT AGATGCTGTT
GAL2kosc.rev: ATT AAT TGT ATG TTA GCT CAG GAA TTC AAC TGG AAG AAA G
Thanks to the lab of Christina Smolke for these primer sequences.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 150
- 1000COMPATIBLE WITH RFC[1000]