SponsoredCRISPR-Cas9 is a genome editing technology used to change parts of the genome. Learn how CRISPR-Cas9 works and discover its advantages and limitations.
SponsoredViral Vector-based & Non-viral Vector-based Delivery Systems Development for Gene Therapy. Lentivirus/Adenovirus/HSV/VACV/AAV Vector, Polyplexes, Dendrimers as Gene Delivery System
Service catalog: Custom miRNA Synthesis, miRNA Inhibitor Synthesis