レンチウイルスプラスミド設計・構築

PackGene offers high-quality lentivirus CRISPR vectors for precise gene editing and regulation. We offer plasmids for the expression of SpCas9, SaCas9, or gRNA, either separately or combined in an all-in-one vector. Our lentivirus Cas9 vector is de novo synthesized on a verified backbone, ensuring reliability and high production yields during lentivirus manufacturing.

Design your lentivirus CRISPR vector via piVector Designer or contact our Ph.D.-level tech support team.

PackGene’s lentivirus shRNA vectors are engineered for gene silencing by expressing shRNA sequences, that are processed into siRNA to target and degrade mRNA. These vectors are important tools for knocking down gene expression and observing phenotypic changes. Additionally, we offer lentivirus shRNA cloning for custom vector construction. To access our lentivirus shRNA vector library and design your vector, please check piVector Designer.

Available upon request, please contact our technical support team to assist your design.

PackGene’s lentivirus miRNA vectors are customizable for overexpression or inhibition of specific miRNAs to provide insights into miRNA-mediated gene regulation. Lentivirus miRNA cloning is a valuable tool for research and developing miRNA-based therapies, particularly in cancer.

Vector design and construction are available upon request, please contact our technical support team.