About the Ultra-Competent Cells Transformation Kit™
The R&R Kit is designed for researchers that want a low-cost, on-demand, rapid, long-shelf-life, and robust transformation tool that is stable in the fridge. It's time to spend less and get more!
- Cost: Traditional ultra-competent cells that you store in the -80 C freezer cost about $13 per transformation reaction. The R&R Kit costs less than half per reaction: 10 rxns kit costs US$6 per reaction, 20 rxns kit costs US$5.50 per reaction, 30 rxns kit costs US$5 per reaction
- On-demand: R&R Kit is stored in the fridge for extended periods of time and can be used at any time. There is no extensive preparation of buffers, measuring pH, or scouring the department for metal salts. Just grab the kit from the fridge and use the contents inside to do the transformation.
- Rapid: The R&R Kit requires 2.5 hours of total time to transform cells, including a 2 hour incubation period where you can go for lunch, actually write your thesis, or set up and run a quick ligation. Actual bench time with the R&R Kit is less than 30 minutes.
- Long shelf-life: The R&R Kit lasts in a fridge for at least 9 months. Traditional ultra-competent cells that you make in-house or buy commercially have an optimal shelf life of days, and if your cells are stored at a temperature above -70 C for even a short period of time the competency drops substantially (does your lab mate leave the -80 door open for extended periods of time?).
- Robust: The transformation efficiency of the R&R Kit is comparable to or even better than traditional ultra-competent cells. For clean plasmid preps, it works phenomenally. For ligation reactions, you’ll typically get several colonies (so long as your ligation was successful!).
Type of DNA |
Expected result (20 min recovery) |
Expected result (overnight recovery) |
Mini-prepped plasmid DNA (1-10 ng/uL) |
100+ CFU |
250 CFU to lawn |
Ligation mix (~10 ng/uL)* |
Up to 50 CFU |
up to 100 CFU |
PCR cleanup Ligation mix (1-10 ng/uL)* |
10+ CFU |
25+ CFU |
*Transformation efficiency is primarily dependent on the restriction sites used, the quality of pre-ligation DNA parts, and the success of the ligation reaction.
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