Part:BBa_K4585008
pGL4.35-3xHA-9xGAL4UAS-KRAB-NLS linearized vector
The objective was to synthesize the pGL4.35-3 HA-9 GAL4UAS-KRAB-NLS plasmid by homologous recombination with the KRAB homologous recombination fragment .
pGL4.35-3×HA-9×GAL4UAS-KRAB-NLS linearized vector
We based on the sequence of the pGL 4.35 plasmid. Through homologous recombination experiments, the Gal 4 sequence, 3 HA sequence were ligated to the pGL 4.35 plasmid, and nine UAS sequences were inserted simultaneously. Special primers were designed, and then the plasmid was cut into linear sequences of a length of about 4500 bp by PCR. The two ends of the linear sequence can be complementary to both ends of the KRAB homologous recombination fragment, and the purpose is to perform homologous recombination with the KRAB homologous recombination fragment to obtain the target product pGL4.35-3 HA-9 GAL4UAS-KRAB-NLS plasmid.
1 Pattern Diagram
Fig.1 The agarose gel electrophoresis of pcDNA3.1(+)-3×HA-Gal4-KRAB-NLS linearized vector
2 Experiment
Based on the sequence of the pcDNA3.1 (+) plasmid, With the help of the GAL 4 homologous recombination fragments and homologous recombination experiments.We designed and synthesized the target product.
3.Caution
The two ends of the pcDNA3.1(+)-3×HA-Gal4-KRAB-NLS linearized vectror need to be complementary to the two ends of the corresponding recombinant fragments to ensure the success of homologous recombination ligation.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 46
Illegal XbaI site found at 85
Illegal SpeI site found at 4849
Illegal PstI site found at 51
Illegal PstI site found at 1480 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 46
Illegal SpeI site found at 4849
Illegal PstI site found at 51
Illegal PstI site found at 1480
Illegal NotI site found at 72 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 46
Illegal BglII site found at 4612
Illegal BamHI site found at 6048
Illegal XhoI site found at 79
Illegal XhoI site found at 5818 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 46
Illegal XbaI site found at 85
Illegal SpeI site found at 4849
Illegal PstI site found at 51
Illegal PstI site found at 1480 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 46
Illegal XbaI site found at 85
Illegal SpeI site found at 4849
Illegal PstI site found at 51
Illegal PstI site found at 1480
Illegal NgoMIV site found at 590
Illegal NgoMIV site found at 1931
Illegal NgoMIV site found at 2216
Illegal AgeI site found at 143 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 5737
Illegal BsaI.rc site found at 3744
Illegal BsaI.rc site found at 5482
Illegal SapI site found at 2661
Illegal SapI.rc site found at 7
Illegal SapI.rc site found at 1780
Illegal SapI.rc site found at 1990
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