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Part:BBa_K4585008

Designed by: Siyao Ma   Group: iGEM23_CSU-CHINA   (2023-10-04)
Revision as of 15:59, 8 October 2023 by Bozjs711 (Talk | contribs)


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 pGL4.35 plasmid. Through homologous recombination experiments, the Gal 4 sequence, 3× HA sequence were ligated to the pGL4.35 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 pGL4.35-3×HA-9×GAL4UAS-KRAB-NLS linearized vector

2 Experiment

Based on the sequence of the pGL4.35-3 plasmid, we designed the pGL4.35-3×HA-9×GAL4UAS-KRAB-NLS linearized vectror by using the GAL 4 homologous recombination fragment, 9×UAS homologous recombination fragment and homologous recombination experiments.

3.Caution

The two ends of the pGL4.35-3×HA-9×GAL4UAS-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.

4. Results

After sequencing and ensuring the sequence was correct, we applied it to the experiments. Store at 4℃.

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