Difference between revisions of "Part:BBa K1680024"

Latest revision as of 02:25, 26 September 2015

Dronpa caged Cre with NLS

This part contains the protein coding region for a fusion protein of Cre recombinase (Part:BBa_K1680007) that is C- & N-terminal flanked with 145N Dronpa part:BBa_K1680006 using a 15 amino acid Ser/Gly-linker part:BBa_K1680003 and the scar (Ser/Thr) as spacer. The construct has an N-terminal NLS sequence part:BBa_K1680004. In the expressed construct the two Dronpa domains should form multimers leading to an inactivated Cre recombinase that is reversibly activatable by Dronpa illumination (see Zhou et al 2012).

This Part is cloned and shipped in the pTUM104 Part:BBa_K801004 and thereby galactose inducible in yeast.

Sequence and Features

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
COMPATIBLE WITH RFC[12]
21
INCOMPATIBLE WITH RFC[21]
Illegal BglII site found at 298
Illegal BglII site found at 2086
23
COMPATIBLE WITH RFC[23]
25
COMPATIBLE WITH RFC[25]
1000
INCOMPATIBLE WITH RFC[1000]
Illegal BsaI site found at 1181

@@ Line 2: / Line 2: @@
 <partinfo>BBa_K1680024 short</partinfo>
-This part contains the protein coding region for a fusion protein of Cre recombinase (BBa_K1680007) that is C- & N-terminal flanked with 145N Dronpa part:BBa_K1680006 using a 15 amino acid Ser/Gly-linker part:BBa_K1680003 and the scar (Ser/Thr) as spacer. The construct has an N-terminal NLS sequence part:BBa_K1680004. In the expressed construct the two Dronpa domains should form multimers leading to an inactivated Cre recombinase that is reversibly activatable by Dronpa illumination (see Zhou et al 2012).
+This part contains the protein coding region for a fusion protein of Cre recombinase ([[Part:BBa_K1680007]]) that is C- & N-terminal flanked with 145N Dronpa [[part:BBa_K1680006]] using a 15 amino acid Ser/Gly-linker [[part:BBa_K1680003]] and the scar (Ser/Thr) as spacer. The construct has an N-terminal NLS sequence [[part:BBa_K1680004]]. In the expressed construct the two Dronpa domains should form multimers leading to an inactivated Cre recombinase that is reversibly activatable by Dronpa illumination (see Zhou et al 2012).
 This Part is cloned and shipped in the pTUM104 [[Part:BBa_K801004]] and thereby galactose inducible in yeast.