
pALD Lenti Products
Lentiviral Vector Plasmids
A solution from early research through commercial development
Aldevron provides pALD-Lenti packaging plasmids through our partnership with OXGENE, who have optimized them for lentiviral vector production. They are immediately available at research grade, GMP-Source™, and cGMP. This will potentially reduce your cost and time to manufacture vectors for clinical trials.
The Aldevron pALD-Lenti system has several advantages:
- Immediately available at Research Grade, GMP-Source and cGMP
- No royalties charged by Aldevron for research through commercial use of plasmids for lentiviral manufacture
- Demonstrated performance producing lentiviral vectors
Provided under license from:

pALD-Lenti System
What's included
We provide three packaging plasmids and an expression plasmid, including:
- pALD-Lenti-EGFP
- pALD-VSV-G
- pALD-GagPol
- pALD-Rev
We can clone your gene of interest into the pALD-Lenti-EGFP expression plasmid, replacing the EGFP sequence.

The system has been optimized and represents the state of the art in lentiviral vector production, including:
- Codon optimization
- Vector backbones minimized
- Minimization of homology with HIV/VSV
- Minimization of inter-cassette homology
In addition to the optimized design, lentiviral vectors produced with the pALD-Lenti system transfect cells with a higher infectious titer than commercially available kits.

- Download the label license for use of pALD Lenti products
- Download a non-confidential transfection protocol without plasmid ratio information
- Request access to sequences and confidential transfection protocol
pALD-Lenti Plasmid Maps
pALD-LentiEGFP-K
pALD-Rev-K
pALD-VSV-G-K
pALD-GagPol-K
Appearance | Clear and Colorless |
Buffer | TE |
USP Sterility <71> * | No Growth |
Concentration | 1.0 mg/mL +/- 10% |
DNA Homogeneity | ≥ 80% Supercoiled |
Endotoxin | ≤ 100 EU/mg |
Identity | Confirmed Against DNA Ladder |
Plasmid Identity | Identical to Reference Sequence |
ABS 260/280 Ratio Purity | 1.80 - 2.00 |
Residual Host Genomic DNA via qPCR | ≤ 5% |
Residual Host Protein via BCA | ≤ 2% |
Residual Host RNA via SYBR Gold | ≤ 5% by Semi-Quantitative Densitometry |
Restriction Digest | Matches Expected Restriction Pattern |
Mycoplasma Contamination | Negative for the Presence of Mycoplasma |
*Sterility testing is not available for research grade material. Bioburden by direct inoculation with a specification of no growth after 48 hours is performed at the research grade level.