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AAV8 Virus-Like Particles (Empty Capsids)

For research use only. Not intended for any clinical use.
Cat.No.
VLP-AAV005
Description
AAV8 virus-like particles are empty capsids of AAV serotype 8 that do not contain any genomic material and can be used as reference materials and other applications.
Shipping
Dry ice
Storage
-80˚C

Background

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Q & A

Customer Reviews

AAV8 stands for adeno-associated virus serotype 8. It is one of the many serotypes of adeno-associated virus (AAV) used in gene therapy. AAVs are small viruses that infect humans and some other primates, but it is not clear whether they cause disease. They are designed to deliver therapeutic genes to cells because they can effectively target specific tissues and have a relatively low risk of causing an immune response. AAV8 is very effective in targeting hepatocytes, making it an attractive option for gene therapies aimed at treating liver-related diseases. It is also able to transduce muscle and some other tissues relatively efficiently. The concept of virus-like particles (VLPs) is used in various fields, including vaccine development, drug delivery, and molecular biology research. These particles mimic the structure of natural viruses without the risk of viral replication or disease transmission, providing a safe and effective platform for a variety of applications. AAV8 virus-like particles are empty capsids of AAV serotype 8 that do not contain any genomic material. In gene therapy studies, empty AAV8 capsids are used as controls in experiments evaluating the efficacy and safety of AAV-based therapies. They help distinguish the effects of the capsid itself from those of the therapeutic gene. Additionally, empty capsids are useful in examining the biodistribution and pharmacokinetics of AAV particles in vivo , providing insight into how these vectors navigate and distribute in biological systems.
Customer Q&As
Can I utilize different serotypes of AAV virus in the same equipment to keep the infected cells?

A: There is no problem with using different serotypes in the same equipment, as long as the handler takes the basic precautions to avoid cross-contamination.

What is the difference between brain localization of gene expression after injection of AAV or lentiviral vectors?

A: Lentiviral particles don't spread well after stereotaxic injection into brain because the particles are relatively large (90nm~100nm). In contrast, AAV particles spread more readily due to smaller size (20nm~100nm). As mentioned, it has been stated that some AAV serotypes spread better than others in brain, for example, AAV5 is reported to spread exceptionally well when injected into striatum. Lastly, pretreatment with mannitol to your animal about 15 min ahead of viral injection has been reported to aid in spread of viral particles in the brain.

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Customer Reviews
Reliable Quality

Reliable quality and ease of use. Because the product undergoes rigorous quality control testing, including ELISA for titration, endotoxin assay, bioburden, SDS-PAGE and silver staining for purity.

United States

05/07/2022

Long-Term Stable Expression

Cteative Biogene offers AAV products that mediate long-term stable expression of genes in vivo.

United States

11/23/2022

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