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"

Revision as of 03:28, 30 October 2008

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PRINCETON IGEM 2008

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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.
pLV-Hef1aLacO-MashI-2A-ChAT-Ubc-Hyg

pLV-Hef1aLacO-MashI-2A-Nurr1-Ubc-Hyg

pLV-Hef1a-LacO-MashI-Cerulean-Ubc-Hyg

pLV-Hef1a-LacO-MashI-EGFP-Ubc-Hyg

pLV-Hef1a-LacO-MashI-Ubc-Hyg

pLV-Hef1a-LacO-MashI-Ubc-Hyg2

pLV-Hef1aLacO-Ngn1-Ubc-Hyg

pLV-Hef1aLacO-Ngn2-Ubc-Hyg

pLV-Hef1aLacO-Nurr1-Ubc-Hyg

pLV-Hef1aLacO-Tlx3-Ubc-Hyg

pLV-pLux-ChAT-Ubc-Neo

pLV-TRE-Cav3.1

pLV-TRE-Cav3.1-Ubc-Bleo

pLV-TRE-D5R-Ubc-Bleo

pLV-TRE-GLRA1-2A-gephyrin-Ubc-Neo

pLV-TRE-GLRA1-Ubc-Neo

pLV-TRE-GLYT2-2A-Viaat-Ubc-Bla

pLV-TRE-HCN2-Ubc-Bla

pLV-TRE-Lbx1-2A-GLRA1-2A-D5R-Ubc-Bla

pLV-TRE-Lbx1-Ubc-Puro

pLV-TRE-MashI-IRES2-mKate

pLV-TRE-Neuregulin1-Ubc-Neo

pLV-TRE-Ngn1-EYFP-Ubc-Bla

pLV-TRE-Ngn1-EYFP-2A-mKate-Ubc-Bla

pLV-Ubc-rtTA-2A-LacIKrab-2A-LuxR-IRES-Puro

pLV-Ubc-rtTA-2A-LacIKrab-IRES-Puro