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Team:MIT phage context
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<b>WORK FROM OTHER IGEM TEAMS</b> | <b>WORK FROM OTHER IGEM TEAMS</b> | ||
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| - | + | In 2006 the McGill team attempted to use leucine zippers fused to split YFP to display on cells and cause the cells to adhere via the split YFP. See: http://parts.mit.edu/wiki/index.php/McGill_University_2006 | |
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| + | The 2009 Freiburg Bioware team used Fos/Jun for a 'programmable enzyme' using Fok-fused Fos/Jun as factor in DNA cleavage. See: https://2009.igem.org/Team:Freiburg_bioware/Project/FOS | ||
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| + | Paris's team in 2009 attempted to use Jun/Fos as a snare; Jun on signal vesicle, Fos on membrane of receiving cell. See: https://2009.igem.org/Team:Paris#top | ||
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Revision as of 19:50, 24 October 2010
iGEM 2010
hairy cells and polymerizing phage - Context |
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WORK FROM OTHER IGEM TEAMS In 2006 the McGill team attempted to use leucine zippers fused to split YFP to display on cells and cause the cells to adhere via the split YFP. See: http://parts.mit.edu/wiki/index.php/McGill_University_2006 The 2009 Freiburg Bioware team used Fos/Jun for a 'programmable enzyme' using Fok-fused Fos/Jun as factor in DNA cleavage. See: https://2009.igem.org/Team:Freiburg_bioware/Project/FOS Paris's team in 2009 attempted to use Jun/Fos as a snare; Jun on signal vesicle, Fos on membrane of receiving cell. See: https://2009.igem.org/Team:Paris#top |
