VIRUS PACKAGING



AAV, LV, and AdV virus packaging, library construction, and cell line development, providing ready-to-use, reliable tools to accelerate gene research and functional studies.





VIRUS PACKAGING

OVERVIEW

Virus packaging services offer high-quality, ready-to-use viral vectors for gene delivery, functional genomics, gene therapy studies, and CRISPR or shRNA library experiments. Our services cover a comprehensive suite of solutions for genetic research, including Adeno-Associated Virus (AAV) packaging, Lentivirus (LV) packaging, Adenovirus (AdV) packaging, library construction, and cell line construction. Our viral vectors are produced under strict quality control, ensuring high titer, purity, and safety, while offering fast production, reproducibility, scalability, and endotoxin-free preparations. Combined with expert support for custom library generation and reliable cell line construction, we provide end-to-end solutions that streamline your experiments, accelerate research workflows, and allow you to focus on scientific discovery.



POPULAR SERVICES OF VIRUS PACKAGING

AAV Packaging

High-quality adeno-associated virus vectors for efficient and safe gene delivery.



LV Packaging

Lentiviral vectors with high titer and reproducibility for stable gene expression.



AdV Packaging

Adenoviral vectors ideal for transient gene expression and large transgene delivery.



Library Construction

Customized CRISPR or shRNA libraries for functional genomics and screening studies.



Cell Line Construction

Stable or inducible cell lines tailored for gene overexpression, knockout, or knock-in experiments.



KEY ADVANTAGES OF VIRUS PACKAGING



High Quality and Safety

Viral vectors are produced under strict quality control with high titer, purity, and endotoxin-free preparations.



Fast Turnaround

Gene synthesis and viral vector packaging delivered in as fast as 15 days.



Comprehensive Solutions

Coverage of AAV, LV, and AdV packaging, plus customized library construction and stable cell line generation for diverse applications.



Research Acceleration

Ready-to-use vectors and expert technical support streamline experimental workflows, enabling faster functional genomics and gene therapy studies.



SERVService Description Titer / Quantity Turnaround Time Applications

AAV Packaging Adeno-Associated Virus packaging service for stable and long-term gene delivery. High-titer, purity-controlled, endotoxin-free viral prep 12~18 business days Gene therapy studies, functional genomics, in vivo experiments

LV Packaging Lentivirus packaging service for efficient gene delivery in dividing and non-dividing cells. High-titer, purity-controlled, endotoxin-free viral prep 15~25 calendar days CRISPR screening, stable cell line generation

AdV Packaging Adenovirus packaging service for high expression and transient gene delivery. High-titer, purity-controlled, endotoxin-free viral prep 55 business days Overexpression studies, vaccine research

Library Construction Custom sgRNA libraries and site-saturation mutagenesis libraries tailored to functional genomics and screening studies. Virus ≥1 mL, >1E+8 TU/mL (typical) Inquiry Genome-wide or pathway-specific functional screens

Cell Line Construction Generation of stable cell lines using packaged viral vectors. Custom deliverables depending on design Inquiry Long-term functional studies, disease modelingICE DETAILS OF VIRUS PACKAGING



WORKFLOW OF VIRUS PACKAGING

Sequence Design & Synthesis: Design and synthesize the DNA sequence (gene or sgRNA cassette) of interest.



Plasmid Preparation: Clone the gene or sgRNA cassette into an appropriate transfer plasmid and prepare high-quality DNA.



Virus Packaging: Introduce plasmids into producer cells to generate viral particles.



Centrifugation / Purification: Clarify, concentrate, and purify the viral supernatant.



Quality Control & Delivery: Measure titer, verify purity, and provide the virus ready for use along with documentation.



APPLICATION OF VIRUS PACKAGING



Gene Delivery & Expression

Efficient, high-titer viral vectors for stable or transient gene delivery in cells.



Functional Genomics & Screening

CRISPR, sgRNA, or mutagenesis libraries for genome-wide or pathway-specific studies.



Disease Modeling & Experimental Research

Stable cell lines and in vivo models to study gene function and therapy.




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