AAV technology
Discover AAVENZENE, a toolkit for gene therapy, and deliver DNA to target cells.
What is AAVENZENE?
Adeno-associated virus (AAV) is a versatile viral vector used as a mechanism of delivery in gene therapy. AAVs are easily adaptable and can be engineered to specifically deliver DNA to target cells.
To develop gene therapies, recombinant AAV (rAAV), which lacks any viral DNA, is used. The use of rAAV in clinical and preclinical applications has proven a safe and effective delivery system. In addition to gene therapy applications, rAAV particles can also be used in in vitro transcription (IVT).
Our AAVENZENE kit includes the essential tools you need to produce your desired rAAV particles, including:
- AAV RepCap plasmid
- AAV helper plasmid
- AAV expression plasmid suitable for cloning the gene of interest (GOI)
Each plasmid encodes key components required to prepare rAAV particles. After the three plasmid (triple) transfection method, the components are expressed and the rAAV particles are produced.
A positive control is also provided with yellow fluorescent protein (YFP) as the GOI.
Why choose AAVENZENE?
Our AAVENZENE kit provides several advantages, including:
- Kanamycin resistance
- Ready to use research-grade plasmids
- Reproducible and reliable rAAV production
- Developed from a scalable and robust RNase-free purification process
We also offer custom-designed research-grade plasmids tailored to suit any GOI.
Partners we work with
Mankind pharma
Ipca
Pharmasyntez
Centurion
Contact us to receive a free AAVENZENE sample
Request a free AAVENZENE sample through our contact form and join the revolution.