Adeno Associated Virus

Adeno-Associated Virus(AAV) Services

AAV vectors tailored to your research, backed by over 30+ years of expertise.

Harnessing AAV for Safe and Targeted Gene Delivery

Adeno-Associated Virus (AAV) is a powerful tool for gene therapy, capable of delivering DNA to target cells with high precision and efficiency. AAV is a non-enveloped virus that has become a gold standard for gene delivery due to its safety and versatility in targeting different cell types.

Key Advantages of AAV

AAV is a preferred gene therapy vector due to its precision, low immune response, and ability to target diverse cell types safely and effectively.

Non-Pathogenic

AAV does not cause any known human disease, making it a safe option for gene delivery.

Low Immunogenicity

Elicits only a mild immune response, reducing the risk of adverse reactions.

Broad Targeting Capability

Can target both dividing and non-dividing cells.

Tissue-Specific Targeting

Different serotypes allow for targeting specific tissues with precision.

AAV Services

Our AAV Services

We specialize in providing high-quality AAV vectors customized to meet your research and therapeutic needs. Our AAV production includes:

01.

High Purity, High Titer Vectors

Available in serotypes 1, 2, 5, 9, and PHP.eb. Other serotypes to follow.

02.

Custom Plasmid Design

Tailored to optimize transgene expression

03.

Vector Production & Purification

Delivered at industry-leading purity & titer levels

04.

Comprehensive Quality Control

Including full/empty capsid ratio and purity testing

05.

Gene-Specific
Titers

Ensuring accurate delivery and expression

01. Personalized Support for Every Project

Not sure which AAV vector is right for your project? Our team of experts provides one-on-one consultation to help you:

Our guidance ensures you achieve the highest levels of efficiency and accuracy in your research.

02. Quality Control & Characterization

We take quality seriously. Every batch of AAV vectors undergoes rigorous testing to ensure consistent performance:

FAQs

Frequently Asked Questions

Got questions? We’ve got answers. Browse through the most common questions to learn more about how we work, what we offer, and how we can help.

AAV vectors should be stored immediately at -80°C. All our vectors have shelf-life of one year without loss in titer.

We recommend not to freeze-thaw your viral vector preparations multiple times. If you plan to use the virus for multiple experiments, thaw the viral preparation on ice, remove the desired volume for use in experiment, aliquot the remaining viral vector preparation into smaller aliquots, and snap-freeze aliquots in dry ice before storing at -80°C.

The maximum gene capacity between the two ITRs of an AAV vector is 4.5kb.

We determined the number of viral genomes/mL of purified prep. This is determined by Absolute Q Digital PCR and/or by UV/vis concentration and Dynamic light scattering UV/Vis (Stunner machine).

AAV vectors

PBS pH 7.4 and 0.001% pluronic acid F68

Why Choose Us for AAV Production?

At Tailored Genes, we’re committed to delivering high-quality AAV vectors with speed, reliability, and personalized support. All of our vectors are manufactured in North America, ensuring compliance with stringent quality standards. Whether you need small-scale production in just one week or large-scale batches in two to three weeks, our streamlined process delivers results fast. We also back every order with a satisfaction guarantee—if something isn’t right, we’ll work closely with you to make it right.

Our Solutions

Explore More Manufacturing Solutions

Expertly crafted virus vectors and cell line solutions—powering research from bench to breakthrough.

Lentivirus Vectors

Transduce any cell with our high titer and high purity LV vectors.

Stable Cell Lines

Overexpress, repress or induce gene expression in cell line of your choice.

CRISPR Vectors

Gene editing, simplified—powered by lentiviral delivery

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