We can design and generate custom CRISPR lentivirus vectors to aid you in your gene-editing goals. We can provide gene-specific knockout, repression, and activation lentivirus vectors using CRISPR constructs, allowing you to manipulate gene expression in your desired host cells. Our CRISPR vectors are fully customizable, and we’ll work with you to come up with a design that meets your needs. We understand that CRISPR editing can be used for an infinite variety of research ambitions, and we can collaborate with you to achieve your individual goals.