Adeno-Associated VIRUS (AAV) Services

 

As cell and gene therapy research continues to advance across a wide-range of diseases, the need for effective vectors for successful therapy delivery has increased. Identified as an optimal vehicle, adeno-associated virus (AAV) plasmids are the leading viral vector used in in vivo gene therapy clinical trials due to their high efficiency and enhanced safety in humans.

As a global leader in genomics services, GENEWIZ has developed unique AAV-ITR sequencing, AAV plasmid synthesis, and AAV plasmid preparation capabilities to support scientists in their in vivo gene therapy research. GENEWIZ’s ground-breaking AAV services also include sequence verification and correction of inverted terminal repeat (ITR) regions, which are crucial for rAAV packaging production. 


AAV Services

AAV-ITR Sequencing

Utilizes Sanger protocols to sequence-confirm difficult ITR regions, expediting screening and validation of lead candidates. Whole AAV plasmid sequencing through primer walking is also available.


AAV Plasmid Preparation

Ensures delivery of intact ITR regions while providing superior quality for mini-to-giga scale AAV vectors.


AAV Plasmid Synthesis

Enables synthesis and cloning of transgene expression cassettes into custom AAV vectors. Includes ITR correction to synthesize and clone correct ITR sequences.


Viral Genome Sequencing

Reimagine quality control standards for rAAV vectors by employing long-read (>10kb) NGS to examine genome integrity, detect heterogeneity, and reveal packaging attributes. Analyze host response utilizing RNA-seq and a variety of other proprietary deep sequencing approaches.


AAV ADVANTAGES

Low cell toxicity as it does not integrate into host genome
Low immunogenicity and non-pathogenic with minimal immune host response
High levels of in vivo gene expression
High transduction efficiency across a broad range of target tissues

AAV SYSTEM

Adeno-associated virus (AAV) is one of the most actively investigated gene therapy vehicles. AAV has a linear single-stranded DNA (ssDNA) genome of approximately 4.7 kilobases (kb), with two 145 nucleotide-long inverted terminal repeats (ITR) at the termini which are crucial for rAAV production. 

Figure 1. An AAV transfer plasmid containing the modified/transgene expression cassette with intact ITRs is generated and cloned into a plasmid along with Rep/Cap and helper plasmids, which are co-transfected into cell lines for virus packaging and rAAV production.

Features & Benefits

  • Building

    Rapid Turnaround Times
    Starting at just 5 business days
  • Building

    Real-Time Project Updates
    Through our online system
  • Building

    Ph.D.-Level Project Managers
    Available at each step


End-to-end DNA AAV solutions with ITR sequencing verification, transgene synthesis, and plasmid preparation
Low immunogenicity and non-pathogenic with minimal immune host response

Robust quality control ensures AAV plasmids are delivered with intact ITRs confirmed via AAV-ITR sequencing

Convenient online ordering directly through your CLIMS account for all services

Technical Resources

Tech Note: Reading Through the Inverted Terminal Repeats (ITRs) of Adeno-associated Virus (AAV)

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.