Interestingly, nano-vectors loaded with Cas9 RNP can directly enter the nucleus to perform CRISPR/Cas9-mediated genome editing. A poly (d,l-lactide-co-glycolide) (PLGA)-based nano-vector for Cas9 ...

In addition, first-generation CRISPR systems (Cas9 and Cas12a) are too large for efficient in vivo delivery via a single adeno-associated viral (AAV) vector. Now, new preclinical research presents ...

Vector offers custom design and manufacturing services for AAV and adenovirus, as well as catalog vectors for overexpression, shRNA, miRNA, and CRISPR. Vector’s products have been referenced in ...

The well-established platform allows for the ability to support the exacting viral vector manufacturing needs of the NCH NK cells created on the hospital's patented universal-donor NK cell platform.