Custom CRISPR Vectors
Gene editing, simplified—powered by lentiviral delivery
High-Performance CRISPR Lentiviral Vectors for Knockout, Repression, and Activation
The expert team at Tailored Genes can manufacture CRISPR lentiviral vectors for gene-specific knockout, repression, and activation — designed for stable, efficient delivery into a wide range of cell types. Whether you’re editing primary cells, stem cells, or building complex models, our vectors are optimized for your specific research goals.
Why Choose CRISPR Lentivirus Vectors?
CRISPR lentivirus vectors combine the precision of gene editing with the stability and efficiency of lentiviral delivery. They’re ideal for long-term gene modulation in hard-to-transfect cells and are widely used in functional genomics, disease modeling, and drug discovery.
Stable Gene Editing
Enables long-term knockout, repression, or activation in dividing and non-dividing cells
Efficient Delivery
High transduction efficiency in primary cells, stem cells, and organoids
Scalable for Screens
Suitable for pooled or arrayed CRISPR screening applications
Reliable Integration
Lentiviral delivery ensures consistent results across replicates and timepoints
CRISPR Services
CRISPR Vector Services
We provide high-quality CRISPR vectors tailored for precise genome editing applications. Our CRISPR vector services include:
01.
High-Titer Lentiviral Delivery Vectors
Tested for efficient transduction and expression.
02.
Stable CRISPR Cell Line Generation
Engineered for reproducible, long-term editing
03.
Assay Development
Test the effects of gene editing in LVV CRISPR transduced cell lines
Why Choose Us for Custom CRISPR Vectors?
- North American Manufacturing – All vectors are produced in North America, ensuring strict quality standards.
- Fast Turnaround Times – We deliver projects quickly and efficiently, ensuring you get what you need without unnecessary delays.
- Satisfaction Guarantee – We follow up after delivery to ensure the vectors meet your expectations. If issues arise, we’ll work with you to resolve them.
Our Solutions
Explore More Manufacturing Solutions
Expertly crafted virus vectors and cell line solutions—powering research from bench to breakthrough.
Adeno-Associated Virus (AAV)
High titer (10¹³ and 10¹⁴ GC/mL) and ultra pure AAV vectors.
Stable Cell Lines
Overexpress or repress gene expression in the cell line of your choice.
Lentivirus Vectors
High titer (10⁸–10⁹ IU/mL) and high purity LV vectors.
