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| Products/Services Used | Details | Operation |
|---|---|---|
| PCR Cloning and Subcloning> | Plasmids were constructed using standard restriction enzyme/ligation-based cloning techniques or directly synthesized and DNA fragments were generated by DNA synthesis (GenScript) or PCR with Q5 polymerase (NEB). | Get A Quote |
Type IIS restriction enzyme-mediated DNA assembly is efficient but has sequence constraints and can result in unwanted sequence scars. To overcome these drawbacks, we developed UniClo, a type IIS restriction enzyme-mediated method for universal and flexible DNA assembly. This is achieved through a combination of vector engineering, DNA methylation using recombinant methylases, and steric blockade using CRISPR-dCas9 technology to regulate this methylation. Type IIS restriction enzyme sites within fragments to be assembled are methylated using recombinant methylases, while the fragment-flanking outer sites are protected from methylation by a recombinant dCas9-sgRNA complex. During the subsequent assembly reaction... More