pE2F-TA-Luc vector (Cat. No.: V006890)

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Basic Information

Note: pE2F-TA-Luc is a signal pathway reporter vector used to monitor E2F-mediated transcriptional activity, which is crucial for studying cell-cycle regulation. It contains four E2F enhancer elements upstream of a minimal TA promoter, controlling the expression of the firefly luciferase reporter gene. This allows quantitative measurement of pathway induction. The vector backbone includes an ampicillin resistance gene for selection in E. coliand is 4882 bp in size.

Name:: pE2F-TA-Luc

Antibiotic Resistance:: Ampicillin

Length:: 4933 bp

Type:: Signal Pathway Reporter Vectors

Replication origin:: ori

Cloning Method:: Enzyme digestion and ligation

Growth Strain(s):: JM108

Growth Temperature:: 37℃

$ 198.2

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Two tubes of lyophilized plasmid will be delivered, each tube is about 5µg.

Resources

Plasmid Protocol

1. Centrifuge at 5,000×g for 5 min.

2. Carefully open the tube and add sterile water to dissolve the DNA: add 20 μl for 5 μg plasmid, and 100 μl for 100 μg plasmid.

3. Close the tube and incubate for 10 minutes at room temperature.

4. Briefly vortex the tube and then do a quick spin to concentrate the liquid at the bottom. Speed is less than 5000×g.

5. Store the plasmid at -20 ℃.

6. The concentration of plasmid re-measurement sometimes differs from the nominal value, which may be due to the position of the lyophilized plasmid in the tube, the efficiency of the re-dissolution, the measurement bias, and adsorption on the wall of the tube, therefore, it is recommended to transform and extract the plasmid before using it

General Plasmid Transform Protocol

1. Take one 100μl of the competent cells and thaw it on ice for 10min, add 2μl of plasmid, then ice bath for 30min, then heat-shock it at 42℃ for 60s, do not stir, and then ice bath for 2min.

2. Add 900μl of LB liquid medium without antibiotics, and incubate at 37℃ for 45min (30℃ for 1-1.5 hours) with 180rpm shaking.

3. Centrifuge at 6000rpm for 5min, leave only 100μl of supernatant to resuspend the bacterial precipitate and spread it onto the target plasmid-resistant LB plate.

4. Invert the plate and incubate at 37℃ for 14h, or at 30℃ for 20h.

5. Pick a single colony into LB liquid medium, add the corresponding antibiotics, incubate at 220rpm for 14h, and extract the plasmid according to the experimental needs and the instructions of the plasmid extraction kit.

References

Zhu Q, Yang J, Han S, et al. Suppression of glycogen synthase kinase 3 activity reduces tumor growth of prostate cancer in vivo. Prostate. 2011;71(8):835-845. doi:10.1002/pros.21300