Resources » Learning Center » Handbooks » Cell and Gene Therapy Handbook
As recent developments in gene and cell therapy continues to advance medicine and drug discovery, the demand for highly customizable, quality assured, full-service providers have mounted. GenScript is proud to work alongside scientists worldwide to bring these tailor-made solutions to you.
With our proven track record, experienced scientists and project management teams and extensive portfolios, GenScript promises top notch services for the most urgent medical and scientific breakthrough.
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CRISPR gRNA/Cas9 and HDR donor solutions for precise and efficient genome editingCustom RNA oligo
High throughput (HT) gene to antibody production offers the most cost-effective option for small-scale recombinant antibodies.
Offers accurate and efficient assembly and cloning of various predefined DNA fragments or parts into a vector of customer choice to generate a library of cloned constructs strategically assembled in a specific arrangement
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.