Team:Princeton/ListofPlasmidDesigns
From 2008.igem.org
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- | [ | + | [https://2008.igem.org/Media:pLV-Hef1a-LacO-MashI-Cerulean-Ubc-Hyg.docx pLV-Hef1a-LacO-MashI-Cerulean-Ubc-Hyg] |
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- | [ | + | [https://2008.igem.org/Media:pLV-TRE-Cav3.1.docx pLV-TRE-Cav3.1] |
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- | [ | + | [https://2008.igem.org/Media:pLV-TRE-GLRA1-2A-gephyrin-Ubc-Neo.docx pLV-TRE-GLRA1-2A-gephyrin-Ubc-Neo] |
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- | [ | + | [https://2008.igem.org/Media:pLV-TRE-MashI-IRES2-mKate.docx pLV-TRE-MashI-IRES2-mKate] |
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Revision as of 01:45, 30 October 2008
PRINCETON IGEM 2008
Home | Project Overview | Project Details | Experiments | Results | Notebook |
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Parts Submitted to the Registry | Modeling | The Team | Gallery |
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The highlight code is as follows:
style="background:yellow; color:black" | yellow: overlap of primers with the DNA style="background:green; color:black" |dark green: restriction site style="background:magenta; color:black" |pink: "junk" sequence to allow restriction enzymes to cut near the end of a strand. style="background:cyan; color:black" |light blue: kozak sequence. style="background:teal; color:black" |dark blue: stop codon. style="background:gray; color:black" |gray: a 2A sequence (the amino acid sequence is cut by the cell) style="background:red; color:black" |red: either a linker to fuse two proteins (where indicated) or a sequence with a restriction site removed by changing a base pair with the primer.