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Adenovirus Packaging
Highly Efficient Transduction, Long-lasting Expression
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Home > Virus Packaging > Adenovirus Packaging
Adenovirus Packaging
Synbio Technologies provides Adenovirus Packaging Services for rapid and efficient gene transfection across a wide range of cell types, including primary cells that are challenging to transfect. Our adenoviral packaging system can accommodate large gene fragments and ensures high-level expression of target genes, making it ideal for various experimental studies.
Highlights
  • High Viral Titers
  • Low Disruption Risk to The Host Genome
  • High-efficiency in Gene Delivery Both In Vitro And In Vivo
  • Ability to Infect Both Dividing & Non-dividing Cells
Service Details
Adenovirus Packaging
Service Types Titer Volume Turnaround Time
RNAi Adenovirus 1*1010 PFU/ml or1*1011 PFU/ml 1ml 50-55 Business Days
sgRNA Adenovirus 1*1010 PFU/ml or1*1011 PFU/ml
Overexpression Adenovirus 1*1010 PFU/ml or1*1011 PFU/ml
QUOTE
Deliverables
Free control virus
Virus liquid, ≥1010 PFU/ml, 200 μL/tube
QC report
FAQs
What are the key components needed for adenovirus packaging?

    The key components needed for adenovirus packaging include:

    - Adenoviral vector plasmids: These contain the genetic material to be delivered.

    - Packaging cell lines: These cells support the production of adenoviral particles.

    - Helper plasmids: These provide necessary adenoviral genes that are not included in the vector plasmid but are required for virus production.

What is the safety concerns related to adenovirus packaging?

    Biohazard risks: Adenoviruses can be pathogenic. Proper containment and safety protocols are essential.

    Immunogenicity: The adenoviral vector can trigger immune responses in the host.

    Insertional mutagenesis: The integration of vector DNA into the host genome could potentially cause harmful effects.

What are the common applications of adenoviral vectors?

    Gene therapy: Correcting defective genes or adding new genes to treat genetic disorders.

    Cancer therapy: Delivering therapeutic genes to target and kill cancer cells.

    Vaccines: Developing vaccines by expressing antigens from pathogens to stimulate an immune response.

More FAQs>>
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