Custom Viral Vector Development Services
End-to-end viral vector design and construction covering vector/serotype selection, expression-cassette optimization, cloning, packaging, purification, and QC. Supports AAV, lentivirus, adenovirus, HSV, vaccinia, and baculovirus with scalable production and documentation for in vitro/in vivo studies and IND-enabling work.

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Creative Biolabs provides end-to-end viral vector design and construction to accelerate gene therapy research. From rational vector/serotype selection and expression-cassette design to cloning, packaging and QC, our platform enables consistent, scalable delivery for in vitro and in vivo studies.
Supported vector families include AAV, lentivirus, adenovirus, HSV, vaccinia and baculovirus, with options for promoters, payload optimization, barcoding and reporter elements to fit your program goals.
Key Features / Benefits
- Broad portfolio: AAV, lentivirus, adenovirus, HSV, vaccinia, baculovirus
- Construct design: promoter/UTR optimization, codon usage, reporters/barcodes
- End-to-end build: cloning → packaging → purification → full QC panel
- Scalable production and documentation to support tech transfer/IND
Relevant Applications
- In vitro gene delivery and stable expression model establishment
- In vivo proof-of-concept and biodistribution studies
- Vector optimization for translational and IND-enabling packages
















