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Transform Your Cloning Workflow with ExSembly™ Cloning MasterMix: Say Goodbye to Vector Linearization
Published On 07/29/2024 3:57 PM
__1596355102.jpg "Transform Your Cloning Workflow with ExSembly™ Cloning MasterMix: Say Goodbye to Vector Linearization")
Revolutionizing Genetic Research
In the rapidly evolving field of genetic research, efficiency and accuracy are two key factors to consider when designing experiments. Researchers worldwide are constantly seeking innovative solutions that streamline processes and yield reliable results. The latest breakthrough, the ExSembly™ Cloning MasterMix invented by Dr. Li and his fellows at Bieberich Lab at University of Maryland Baltimore County, addresses these needs by eliminating a traditionally time-consuming step: DNA vector linearization. With this revolutionary technology, scientists can now enjoy faster, more efficient cloning workflows without compromising on quality.
The ExSembly™ cloning technology enables directional insertion of any amplified DNA product into CIRCULAR vector. It completely eliminates the time-consuming step of preparing linear vector. The creative buffer system in the master mix allows restriction enzymes to efficiently digest the circular DNA and maintain high exonuclease and polymerase activity to enable the assembly to occur. Once the vector DNA is successfully assembled with DNA inserts, the restriction sites in the vector disappear, allowing the enzymes to robustly remove background negative clones by completely digesting unassembled vector DNA. One can conveniently use a relatively large amount of vector DNA, up to 500 ng, and obtain a high number of positive clones, which consequently increases success rate.
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Why ExSembly™ Cloning MasterMix?
- One-Step Simplicity: Say goodbye to the DNA vector linearization process and welcome to the one-tube, single-step assembly method that simplifies your cloning workflow. This means you can proceed directly to vector insertion, saving valuable time and reducing the potential for error.
- Unprecedented Speed: Traditional cloning methods typically require vector digestion and gel purification, consuming 2-3 hours of precious research time. ExSembly™ Cloning MasterMix eliminates these steps, allowing you to achieve your cloning goals much faster.
- Superior Efficiency and Low Background: Achieve >95% accuracy with correctly inserted DNA fragments. Our technology employs restriction enzymes that remove background negative clones by fully digesting unassembled vector DNA, ensuring that your results are both reliable and reproducible.
- Scalability: Whether you're assembling a single DNA fragment or multiple fragments, ExSembly™ Cloning MasterMix handles large-scale projects with ease. This scalability makes it a versatile tool for a wide range of applications.
- High Concentration Capabilities: Use up to 500 ng of vector DNA and obtain a high number of positive clones. This flexibility increases your success rate and accelerates your research progress.
- Cost-Effective: By eliminating the need for vector digestion, gel electrophoresis, and purification, ExSembly Cloning MasterMix cuts costs by up to 50%. This cost-efficiency enables you to allocate resources more effectively, further enhancing your research capabilities.
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Performance Compared to Competitors
| Amount of vector DNA | Number of positive colonies | Assembling efficiency | Number of total colonies | |
| Competitor A | 500 ng | 0 | 0 | ~500 |
| 1,000 ng | ~150 | 12.5% | ~1,200 | |
| Competitor B | 500 ng | 0 | 0 | ~300 |
| 1,000 ng | 0 | 0 | ~600 | |
| ExSemblyTM | 500 ng | 35 | 3.5% | ~1,000 |
| 1,000 ng | ~450 | 25% | ~1,800 |
Join the Future of Cloning Today
Our technology is patented in Japan and pending patent in the USA. We understand that transitioning from traditional methods can be challenging, which is why we're offering free samples of ExSembly™ Cloning MasterMix. Experience the benefits firsthand and see how this product can transform your cloning workflow.
>> Click Here to Request Free Samples
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Application and Technique Notes
