Team:Princeton/ListofPlasmidDesigns
From 2008.igem.org
(Difference between revisions)
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The highlight code is as follows: | The highlight code is as follows: | ||
- | style="background:yellow; color:black" | yellow: overlap of primers with the DNA | + | {|align="left" |
- | style="background:green; color:black" |dark green: restriction site | + | |style="background:yellow; color:black" | yellow: overlap of primers with the DNA |
- | 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. | + | {|align="left" |
- | style="background:gray; color:black" |gray: a 2A sequence (the amino acid sequence is cut by the cell) | + | |style="background:green; color:black" |dark green: restriction site |
- | 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. | + | |} |
+ | |||
+ | {|align="left" | ||
+ | |style="background:magenta; color:black" |pink: "junk" sequence to allow restriction enzymes to cut near the end of a strand. | ||
+ | |} | ||
+ | |||
+ | {|align="left" | ||
+ | |style="background:cyan; color:black" |light blue: kozak sequence. | ||
+ | |} | ||
+ | |||
+ | {|align="left" | ||
+ | |style="background:teal; color:black" |dark blue: stop codon. | ||
+ | |} | ||
+ | |||
+ | {|align="left" | ||
+ | |style="background:gray; color:black" |gray: a 2A sequence (the amino acid sequence is cut by the cell) | ||
+ | |} | ||
+ | |||
+ | {|align="left" | ||
+ | |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. | ||
+ | |} | ||
+ | |||
+ | |||
+ | |||
+ | |||
+ | |||
+ | |||
+ | |||
{|align="center" | {|align="center" | ||
- | |[ | + | |[https://2008.igem.org/Media:pLV-Hef1aLacO-MashI-2A-ChAT-Ubc-Hyg.pdf pLV-Hef1aLacO-MashI-2A-ChAT-Ubc-Hyg] |
- | [ | + | [https://2008.igem.org/Media:pLV-Hef1aLacO-MashI-2A-Nurr1-Ubc-Hyg.pdf pLV-Hef1aLacO-MashI-2A-Nurr1-Ubc-Hyg] |
- | [ | + | [https://2008.igem.org/Media:pLV-Hef1a-LacO-MashI-Cerulean-Ubc-Hyg.pdf pLV-Hef1a-LacO-MashI-Cerulean-Ubc-Hyg] |
- | [ | + | [https://2008.igem.org/Media:pLV-Hef1a-LacO-MashI-EGFP-Ubc-Hyg.pdf pLV-Hef1a-LacO-MashI-EGFP-Ubc-Hyg] |
- | [ | + | [https://2008.igem.org/Media:pLV-Hef1a-LacO-MashI-Ubc-Hyg.pdf pLV-Hef1a-LacO-MashI-Ubc-Hyg] |
- | [ | + | [https://2008.igem.org/Media:pLV-Hef1a-LacO-MashI-Ubc-Hyg2.pdf pLV-Hef1a-LacO-MashI-Ubc-Hyg2] |
- | [ | + | [https://2008.igem.org/Media:pLV-Hef1aLacO-Ngn1-Ubc-Hyg.pdf pLV-Hef1aLacO-Ngn1-Ubc-Hyg] |
- | [ | + | [https://2008.igem.org/Media:pLV-Hef1aLacO-Ngn2-Ubc-Hyg.pdf pLV-Hef1aLacO-Ngn2-Ubc-Hyg] |
- | [ | + | [https://2008.igem.org/Media:pLV-Hef1aLacO-Nurr1-Ubc-Hyg.pdf pLV-Hef1aLacO-Nurr1-Ubc-Hyg] |
- | [ | + | [https://2008.igem.org/Media:pLV-Hef1aLacO-Tlx3-Ubc-Hyg.pdf pLV-Hef1aLacO-Tlx3-Ubc-Hyg] |
- | [ | + | [https://2008.igem.org/Media:pLV-pLux-ChAT-Ubc-Neo.pdf pLV-pLux-ChAT-Ubc-Neo] |
- | [ | + | [https://2008.igem.org/Media:pLV-TRE-Cav3.1.pdf pLV-TRE-Cav3.1] |
- | [ | + | [https://2008.igem.org/Media:pLV-TRE-Cav3.1-Ubc-Bleo.pdf pLV-TRE-Cav3.1-Ubc-Bleo] |
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- | [ | + | [https://2008.igem.org/Media:pLV-TRE-D5R-Ubc-Bleo.pdf pLV-TRE-D5R-Ubc-Bleo] |
+ | |||
+ | [https://2008.igem.org/Media:pLV-TRE-GLRA1-2A-gephyrin-Ubc-Neo.pdf pLV-TRE-GLRA1-2A-gephyrin-Ubc-Neo] | ||
- | [ | + | [https://2008.igem.org/Media:pLV-TRE-GLRA1-Ubc-Neo.pdf pLV-TRE-GLRA1-Ubc-Neo] |
- | [ | + | [https://2008.igem.org/Media:pLV-TRE-GLYT2-2A-Viaat-Ubc-Bla.pdf pLV-TRE-GLYT2-2A-Viaat-Ubc-Bla] |
- | [ | + | [https://2008.igem.org/Media:pLV-TRE-HCN2-Ubc-Bla.pdf pLV-TRE-HCN2-Ubc-Bla] |
- | [ | + | [https://2008.igem.org/Media:pLV-TRE-Lbx1-2A-GLRA1-2A-D5R-Ubc-Bla.pdf pLV-TRE-Lbx1-2A-GLRA1-2A-D5R-Ubc-Bla] |
- | [ | + | [https://2008.igem.org/Media:pLV-TRE-Lbx1-Ubc-Puro.pdf pLV-TRE-Lbx1-Ubc-Puro] |
- | [ | + | [https://2008.igem.org/Media:pLV-TRE-MashI-IRES2-mKate.pdf pLV-TRE-MashI-IRES2-mKate] |
- | [ | + | [https://2008.igem.org/Media:pLV-TRE-Neuregulin1-Ubc-Neo.pdf pLV-TRE-Neuregulin1-Ubc-Neo] |
- | [ | + | [https://2008.igem.org/Media:pLV-TRE-Ngn1-EYFP-Ubc-Bla.pdf pLV-TRE-Ngn1-EYFP-Ubc-Bla] |
- | [ | + | [https://2008.igem.org/Media:pLV-TRE-Ngn1-EYFP-2A-mKate-Ubc-Bla.pdf pLV-TRE-Ngn1-EYFP-2A-mKate-Ubc-Bla] |
- | [ | + | [https://2008.igem.org/Media:pLV-Ubc-rtTA-2A-LacIKrab-2A-LuxR-IRES-Puro.pdf pLV-Ubc-rtTA-2A-LacIKrab-2A-LuxR-IRES-Puro] |
- | [ | + | [https://2008.igem.org/Media:pLV-Ubc-rtTA-2A-LacIKrab-IRES-Puro.pdf pLV-Ubc-rtTA-2A-LacIKrab-IRES-Puro] |
- | } | + | |} |
Latest revision as of 03:58, 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:
yellow: overlap of primers with the DNA |
dark green: restriction site |
pink: "junk" sequence to allow restriction enzymes to cut near the end of a strand. |
light blue: kozak sequence. |
dark blue: stop codon. |
gray: a 2A sequence (the amino acid sequence is cut by the cell) |
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. |