AAV Plasmid Preparation

GENEWIZ AAV Plasmid Preparation service delivers superior quality for midi to giga-scale AAV vectors, while maintaining the integrity of ITR regions. Preserving the integrity of inverted terminal repeat (ITR) sequences in adeno-associated virus (AAV) plasmids is important for the production of recombinant AAV (rAAV) vectors. Our new process includes pre- and post-preparation quality controlled (QC) steps that leverage GENEWIZ’s AAV-ITR Sanger sequencing capabilities for full sequence verification and ensures delivery of intact ITR clones for your research.

Preserve ITR INTEGRITY in AAV Vectors

Truncated ITRs can reduce the yield of full viral capsid production and increase generation of undesirable non-rAAV encapsidated DNA. Unfortunately, AAV plasmid ITRs are frequently mutated during plasmid production in bacterial cells. GENEWIZ AAV plasmid preparation service incorporates a two-step QC process, including pre-prep and post-prep QC. The pre-prep QC step assesses your sample configuration for the presence of full-length intact or truncated ITRs, or a mixture of both. This allows selected propagation of intact ITR sub-populations only, while the post-prep QC step ensures integrity of ITR regions in the final plasmids delivered to you. For whole plasmid sequencing, utilize our primer walking service with AAV plasmid preparation.

AAV Plasmid Prep Workflow

*Plasmid DNA is currently the only starting material accepted

Note: Screening and selection of intact ITR clones incurs additional cost

Features & Benefits

  • Robust 2-step QC process with sequence verification using our proprietary AAV-ITR sequencing.
  • Turnaround time starting at 6 business days** with Ph.D.-level support throughout project.
  • High-quality midi- to giga-scale preps available.
  • High success rate compared to standard plasmid preparation kits and protocols.
  • Multiple analysis options available, including sterility testing, restriction digest, full plasmid sequencing, etc.
  • Screening process to isolate intact ITRs in mixed populations.

**6-day turnaround time for samples that have previously been ITR sequence verified at GENEWIZ.

Technical Resources

  • Thumbnail for tech note titled Optimizing Plasmid Preparation to Increase Yield and Reduce Endotoxins

    Tech Note | Optimizing Plasmid Preparation to Increase Yield and Reduce Endotoxins

    Plasmid DNA (pDNA) is vital for a range of biopharmaceutical and biotechnological applications but maximizing yield while minimizing endotoxins can be challenging. This tech note explores strategies to optimize bacterial growth conditions, enhance lysis, and refine purification protocols to boost pDNA yield and purity, ensuring consistent, high-quality results.

  • Thumbnail for tech note titled An Efficient and Reliable Approach to AAV Packaging

    Tech Note | An Efficient and Reliable Approach to AAV Packaging

    While AAV is a powerful vehicle for gene delivery, unstable ITRs threaten the fidelity of rAAV genomes. Loss of ITR integrity diminishes the packaging efficiency of rAAV particles and thus viral titer. In this tech note, discover the effect of partial and full ITR deletions on AAV packaging and how to reliably identify and effectively correct them.

  • Thumbnail for tech note titled An Efficient and High-Fidelity Approach to AAV Plasmid Preparation

    Tech Note | An Efficient and High-Fidelity Approach to AAV Plasmid Preparation

    GENEWIZ has recently developed a proprietary AAV plasmid preparation process, which significantly improves the chance of maintaining ITR integrity, even when other commercially available competent cells growing in low temperature have failed. This process can also isolate clones with full-length ITR from a sample mixture containing intact and truncated ITRs.

  • Thumbnail for tech note titled AAV-ITR Sequencing

    Tech Note | AAV-ITR Sequencing

    GENEWIZ has developed a high-quality, direct Sanger sequencing method that reads through both intact and commonly mutated inverted terminal repeat (ITR) regions of adeno-associated virus (AAV). This method is an effective tool for assessing the integrity of ITRs in AAV plasmids.