Difference between revisions of "Part:BBa K1467100:Experience"
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This experience page is provided so that any user may enter their experience using this part.<BR>Please enter | This experience page is provided so that any user may enter their experience using this part.<BR>Please enter | ||
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===Applications of BBa_K1467100=== | ===Applications of BBa_K1467100=== | ||
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+ | iGEM14_NRP-UEA-Norwich have used this part to convert GoldenGate "Pro + 5U" (promoter and 5' untranslated leader) modules from the GoldenGate MoClo Assembly Standard into standard BioBricks. The cloning reaction was a Golden Gate one-step, one-pot reaction where the restriction enzyme, ligase and (intact, uncut) donating and recipient plasmids were all incubated together in a single reaction before transformation into competent ''E.coli'' cells. Cloning was very successful as the vast majority of the colonies are white as the RFP sequence was replaced by the new part. | ||
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+ | [[Image:Pro-Flipper Chracterisation.jpg|600px|]] | ||
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===User Reviews=== | ===User Reviews=== |
Revision as of 09:57, 6 October 2014
This experience page is provided so that any user may enter their experience using this part.
Please enter
how you used this part and how it worked out.
Applications of BBa_K1467100
iGEM14_NRP-UEA-Norwich have used this part to convert GoldenGate "Pro + 5U" (promoter and 5' untranslated leader) modules from the GoldenGate MoClo Assembly Standard into standard BioBricks. The cloning reaction was a Golden Gate one-step, one-pot reaction where the restriction enzyme, ligase and (intact, uncut) donating and recipient plasmids were all incubated together in a single reaction before transformation into competent E.coli cells. Cloning was very successful as the vast majority of the colonies are white as the RFP sequence was replaced by the new part.
User Reviews
UNIQ4838f52e743d5961-partinfo-00000000-QINU UNIQ4838f52e743d5961-partinfo-00000001-QINU