Figure 3: Characterization of the split AAV vector heterodimerization by RT–PCR and DNA-PCR. There are many potential applications for using SAVE to carry large genes of therapeutic benefit for ...

Researchers can insert DNA fragments or genes into a plasmid vector, creating a so-called recombinant plasmid. This plasmid can be introduced into a bacterium by way of the process called ...

The DNA of interest is first isolated, then combined with a carrier DNA molecule called a vector, which is then introduced into the host organism. Gene editing techniques, such as CRISPR-Cas9, allow ...

The process of creating adenoviral vectors involves inserting the transgene into a small shuttle plasmid so that the transgene cassette can be excised with two restriction enzymes with almost unique ...

Circio Holding ASA, a biotechnology company developing circular RNA technology for next-generation nucleic acid medicine, has ...