AAV Production Service for ay specific gene, shRNA or miRNA

AAV

Safely & efficiently deliver target genes into your cells

Adeno-associated virus (AAV) is a non-enveloped virus that can be engineered to efficiently deliver DNA sequences of interest into target cells with a low immunogenicity. Because of these unique characteristics, AAV-mediated genome editing has emerged as a highly promising gene delivery method.

AMSBIO provides a service to make ready-to-use AAV for any specific gene, shRNA or miRNA. We will sub-clone your selected genes into our AAV expression vectors and produce expression AAV for each gene.

Our Services

Over-expression AAV construction

You can choose the promoter and a tag.

Either you provide target templates or we synthesize or obtain it from a cDNA collection. We construct the AAV clone and generate ready-to-use expression AAV. High titer AAV service is available.

Ensure that you choose the right AAV serotype for your application.

Why use AMSBIO's AAV services?

      • Transfect both dividing and non-dividing cells
      • No host-genome integration & stable expression
      • Easy to produce at high viral titre (helper free)
      • Does not elicit significant immune response in vivo
      • Can be used for in vivo gene delivery

Serotype Selection

Tissue TypeRecommended AAV Serotypes
MuscleAAV1, AAV6, AAV8, AAV9
LiverAAV8, AAV9, AAV-DJ
LungAAV5, AAV6, AAV9
Central Nervous SystemAAV1, AAV5, AAV8, AAV9, AAV-DJ
RetinaAAV1, AAV2, AAV5, AAV8
PancreasAAV8
KidneyAAV2, AAV9
HeartAAV1, AAV8, AAV9

Lentivirus & Adenovirus & AAV Request Form

Let's get started

Complete our service request form and we will contact you to discuss your requirements.