Cell and Gene Therapy Handbook

Lentiviral vectors represent a new vector system that can achieve permanent integration of the gene into dividing and non-dividing cells. The ability to stably integrate at random genomic positions make lentiviral vectors a unique and ideal tool for studying gene’s function in target cells or tissues.

Powered by GenScript's strong expertise in de novo gene synthesis and our semiconductor-based oligo synthesis technology, our Precision Mutant Library service offers precise control over each synthesized variant. The result is a more diverse and fully covered mutant library with unbiased distribution, ultimately saving valuable screening time, speeding up discovery workflow and reducing overall downstream expenses.