



AAV13 Reference (Byproduct-Empty)
Price range: $299.00 through $1,799.00
AAV13 Reference (Byproduct-Empty) particles are byproducts of regular AAV13-CMV-EGFP-2.8kb vectors produced with our pAAVone-AAV13-CMV-EGFP-2.8kb plasmid. Unlike AAV truly-empty particles, AAV byproduct-empty particles may contain partial or incomplete genomes [Wang et al., 2016]. They are not completely devoid of genetic material, and this genetic content can vary in terms of completeness. Byproduct-empty AAV particles are not the primary focus of production and can sometimes be considered impurities or contaminants in the final AAV vector preparation.
- SKU: DF001001-AAV13
- AAV Serotype: AAV13
- AAV Capsid titer: 1.0×1013 VP/ml (VP: Viral Particle) by Elisa
- Used cell line: HEK 293T
- Used plasmid: pAAVone-AAV13-CMV-EGFP-2.8kb
- AAV Genome: AAV-CMV-SV40I-EGFP-WPRE-hGHpolyA-2.8kb
- Production system: AAVone® [Yang et al., 2025]
- Purification: AAVx followed by one round of CsCl ultracentrifuge.
- Buffer: 0.001% F-68/DPBS with additional 150mM NaCl.
- Endotoxin: <1.o EU/1.0×1013 VP
- Storage: -80°C for long term (> 1 year); -20°C for short term(1-2 months); 4 °C for 1-2 weeks..
- Shipping: Dry ice.
AAV References at AAVnerGene:
AAV references (Full) and AAV references (Byproduct-Empty) are generated using the AAVone system, with the corresponding pAAVone plasmids carrying a 2.8 kb AAV-CMV-SV40I-EGFP-WRRE-hGHpolyA genome. AAV references (Truly-Empty) are produced by transfection of a single mini-pHelper-AAV plasmid with the corresponding serotypes. AAV reference materials are available for various serotypes, including AAV1, AAV2, AAV3B, AAV5, AAV6, AAV7, AAV8, AAV9, AAVrh.10, AAV11, AAV12, AAV13, AAVrh.74, AAV2-Retro, AAV-DJ, and AAV-PHP.eB.
| AAV References | Serotype | Genome | Production Plasmids |
| AAV References-2.8kb | AAV1, AAV2, AAV3B, AAV5, AAV6, AAV7, AAV8, AAV9, AAVrh.10, AAV11, AAV12, AAV13, AAVrh.74, AAV2-Retro, AAV-DJ, and AAV-PHP.eB | Full of AAV-CMV-SV40I-EGFP-WPRE-hGHpolyA-2.8kb | pAAVone-AAVs-CMV-EGFP-2.8kb |
| AAV References-4.3kb | AAV1, AAV2, AAV3B, AAV5, AAV6, AAV7, AAV8, AAV9, AAVrh.10, AAV11, AAV12, AAV13, AAVrh.74, AAV2-Retro, AAV-DJ, and AAV-PHP.eB | Full of AAV-CMV-SV40I-EGFP-WPRE-hGHpA-4.3kb | pAAVone-AAVs-CMV-EGFP-4.3kb |
| AAV References (Truly-Empty) | AAV1, AAV2, AAV3B, AAV5, AAV6, AAV7, AAV8, AAV9, AAVrh.10, AAV11, AAV12, AAV13, AAVrh.74, AAV2-Retro, AAV-DJ, and AAV-PHP.eB | No | mini-pHelper-AAVs |
| AAV References (Byproduct-Empty) | AAV1, AAV2, AAV3B, AAV5, AAV6, AAV7, AAV8, AAV9, AAVrh.10, AAV11, AAV12, AAV13, AAVrh.74, AAV2-Retro, AAV-DJ, and AAV-PHP.eB | Partial of AAV-CMV-SV40I-EGFP-WPRE-hGHpolyA-2.8kb | pAAVone-AAVs-CMV-EGFP-2.8kb |
Usage of Empty AAV particles:
Empty AAV particles can serve as valuable tools for various stages of gene therapy development and characterization.
- Reference Materials: Well-characterized empty AAV capsids, can serve as standardized reference materials for analytical assays.
- Quality Control: During the manufacturing process of AAV vectors, using well-characterized capsids as reference materials allows manufacturers to monitor and ensure the quality, purity, and consistency of their AAV products.
- Biodistribution Studies: Empty AAV can be used in biodistribution studies to assess how different capsids distribute in various tissues after administration.
- Immunogenicity Assessment: By exposing the immune system to well-characterized AAV capsids, researchers can evaluate the immune responses induced by specific serotypes..
- Comparative Studies: Empty AAV allow researchers to compare the characteristics of different AAV serotypes without the confounding effects of transgene expression.
- Process Development: Empty AAV can be used in the development and optimization of manufacturing processes for AAV vectors.
- Assay Development: Empty AAV capsids serve as positive controls in various assays, aiding the development of new methods for AAV characterization, stability testing, and potency determination.
- Gene Therapy Capsid Decoys: The presence of an excess of empty AAV capsids may effectively absorb low-level neutralizing antibodies (NAbs) and non-NAbs, permitting transduction even in their presence.
References:
Wang Q, et al., Syngeneic AAV Pseudo-particles Potentiate Gene Transduction of AAV Vectors. Mol Ther Methods Clin Dev. 2016 Dec 24;4:149-158. doi: 10.1016/j.omtm.2016.12.004. eCollection 2017 Mar 17. PMID:28345000
Yang et al., AAVone: A Cost-Effective, Single-Plasmid Solution for Efficient AAV Production with Reduced DNA Impurities.
| Volume Size | 100 μL, 200 μL, 500 μL, 1000 μL |
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