Transfected Stable Cell Lines
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Cat. No. : VLP-AAV005
| 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. |
| Applications | Adeno-associated virus serotype 8 (AAV8) virus-like particles (empty capsids), also known as AAV8 VLPs, have several important applications in gene therapy and related research. Here are some of the main uses: Antibody production: They can be used to produce antibodies against AAV8 capsids, which is essential for developing assays to track immune responses to AAV-based gene therapies. Immune response analysis: Researchers use empty capsids to study how the immune system responds to viral components without the confounding influence of the therapeutic gene. Quality control in AAV production: During the manufacture of AAV vectors for gene therapy, it is important to distinguish between intact capsids (containing the therapeutic gene) and empty capsids. Empty capsids can be used as standards in quality control assays to ensure the purity of the therapeutic vector. Toxicology studies: Before administering gene therapy to humans, it is critical to assess the safety of the delivery vehicle. Empty capsids can be used to study the biodistribution, toxicity, and clearance of viral particles, independent of the transgene. Control experiments: Empty capsids serve as an important control in an experimental setup, ensuring that the observed effects are caused by the therapeutic gene and not the viral capsid itself. |
| Storage | -80˚C |
| Shipping | Dry ice |
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.
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.
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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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.
Cteative Biogene offers AAV products that mediate long-term stable expression of genes in vivo.
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